Cerebral Palsy and Neurodisability
STRUCTURAL CHANGES IN BRAIN ON CRANIAL MAGNETIC RESONANCE IMAGING (MRI) IN SEVERELY MALNOURISHED CHILDREN | |
Harshit Bhargava |
Acute cerebral venous thrombosis and diffuse white matter changes in classic homocystinuria | |
Christopher Barton |
Acetazolamide induced aseptic meningitis in a female adolescent with idiopathic intracranial hypertension | |
Christopher Barton |
Intramyocellular lipid excess in the mitochondrial disorder MELAS: MRS determination at 7T. | |
Sailaja Golla, Craig Malloy, Jimin Ren, Juan Pascual |
Autism Spectrum Disordes - what are we waiting for? : 5 year follow-up study | |
taras no voloshyn |
Fine motor functioning and speech in patients with Autism spectrum disorders during treatment by Intensive Neurophysiological Rehabilitation System | |
Volodymyr no Kozyavkin |
Acetazolamide for severe early-onset epileptic encephalopathy due to mutations in the KCNA2 gene | |
khalid jama hundallah |
Applying the SCPE Brain MRI Classification System in Cerebral Palsy: a valid process for analyzing data from a Cerebral Palsy Registry. | |
Antigoni Syrigou Papavasileiou, Maria Koutsaki, Marianna Petra, Sotiria Mastroyianni, Maria Pyrgelli, George Damianos, Irene Nikaina, Helen Skouteli, Argirios Dinopoulos |
Prevention and Cure of the Intrathecal Baclofen Pump . | |
Yasser Awaad |
Synergetic effect of intrathecal baclofen and deep brain stimulation in treating dystonia | |
Yasser Awaad |
Functional Assessment Following Intrathecal Baclofen Therapy in Children with Spastic Cerebral Palsy | |
Yasser Awaad |
Botulinum toxin- A in postoperative pediatric stiff hips | |
Yasser Awaad |
EFFICACY OF DEEP BRAIN STIMULATION(DBS) IN REFRACTORY PEDIATRIC DYSTONIA | |
Dr Tarishi Nemani, Dr Vishal Kanubhai Patel, Dr.Puja Mehta, Dr.Paresh Doshi, Dr.Anaita Udwadia Hegde |
Bilateral Actigraphy as a Real-World Measure of Motor Asymmetry in Hemiparetic Children with Perinatal Stroke | |
Asha Hollis, Ephrem Zewdie, Adam Kirton |
Frequency and predictive factors of scoliosis in Malaysian children with Cerebral Palsy | |
POORANI ANANDAKRISHNAN, TEIK BENG KHOO |
Improving epilepsy control among children with Cerebral Palsy in rural Bangladesh | |
Tasneem Karim, Manik Chandra Das, Mohammad Muhit, Nadia Badawi, Gulam Khandaker, Shekeeb S Mohammad |
Cognitive profile in children with bilateral spastic cerebral palsy due to periventricular leukomalacia | |
Kaeko Ogura, Yukihiro Kitai, Satori Hirai, Hiroshi Arai |
Upper Limb Habilitation in Children with Hemiplegic Cerebral Palsy Using A Novel Robotic Device – Assessment Using Jebsen-Taylor and Bruininks-Oseretsky Tests | |
Hian-Tat ONG, Hian-Tat ONG, Jia Xuan Tan, Michelle Lee, Jeremy LIN, Chee Leong Teo, Etienne Burdet, Sam Shuzhi Ge |
Long-term neurodevelopmental outcomes following Extracorporeal Life Support and the role of neuroimaging in predicting outcomes | |
Sailaja Golla, Lakshmi Raman, Archana Dhar, Pilar Martin, Mary Ann Morris, Jefferson Tweed, stacey scott, Vinai Modem |
An Update of Epidemiology of Cerebral Palsy in Northern region of Bangladesh – A comparative analysis | |
Mohammad Abdul Wahed |
An Update of Epidemiology of Cerebral Palsy in Northern region of Bangladesh – A comparative analysis | |
Mohammad Abdul Wahed |
CT Scanning findings in clinically diagnosed Cerebral Palsy | |
Mohammad Abdul Wahed |
Wasting Syndrome – A predictor of early death in Cerebral Palsy | |
Mohammad Abdul Wahed |
Mobius syndrome in four cases and literature review | |
yang xinying |
International classification of function (ICF) Its application in cerebral palsy and Validation of the core sets in the Pakistani population | |
Shahnaz Hamid Ibrahim |
Association of Risk factors for Early Childhood Disability in Rural Pakistan | |
Shahnaz Hamid Ibrahim |
Outcomes and SLC2A1 Mutations in Febrile Young Infants with Hypoglycorrhachia | |
WENHAO YU |
ROLE OF LINGUISTIC PROFILING INASSESSMENTS OF LEARNING AND LANGUAGE DISORDERS IN INDIAN CHILDREN-A CASE CONTROL STUDY | |
MsNitya Raman, MONA GAJRE, DrNandini Singh |
A qualitative study on the clinical, radiological characteristics, and Prevalence of co-morbid conditions in children with hemiplegic cerebral palsy | |
Tandra Harish Varma, PRATIBHA SINGHI, Naveen Sankhyan, Prabhjhot Malhi |
Sensorimotor robotic measures of tDCS and HD-tDCS enhanced motor learning in children | |
Lauran Cole |
Sleep Disorders in Children with Cerebral Palsy | |
Tanmay Sanjay Jadhav, Dr. Shilpa Kulkarni, Dr. Amit Bhondve |
CASE CONTROL STUDY ON ANTHROPOMETRIC ASSESSMENT OF CHILDREN WITH CEREBRAL PALSY | |
Aritra Guha, Dipankar Gupta, Sankar Kumar Das |
Prevalence and profile of sleep disorders in children with static encephalopathy (Cerebral palsy) at a tertiary care pediatric centre | |
lakshmi narayana indana, Ramesh Konanki, Lokesh Lingappa, Nikith Milind Shah, Raju B.S.C.P B |
Brain computer interface control in hemiparetic children with perinatal stroke | |
Zeanna Jadavji, Jack Zhang, Ephrem Zewdie, Adam Kirton |
Preliminary Magnetoencephalography (MEG) Findings of Somatosensory Gating Using Dual-Pulse Sensory Tactile Stimulation in Dystonic Children with Basal Ganglia Stroke | |
Nomazulu Dlamini, Ahmad Mousa, Cecilia Jobst, Sabah Master, Gabrielle deVeber, Douglas Cheyne |
Influence of plantar flexors spasticity on center of mass during walking among children with unilateral spastic cerebral palsy | |
Ehab Anwar Waly, Mai Ahmed |
Genomic analysis identifies pathogenic variants in 9 of 17 cases with full-term cerebral palsy | |
Yusuke Takezawa, Atsuo Kikuchi, Kazuhiro Haginoya, Tetsuya Niihori, Yurika Numata-Uematsu, Takehiko Inui, Saeko Yamamura-Suzuki, Takuya Miyabayashi, Mai Anzai, Sato Suzuki-Muromoto, Yukimune Okubo, Wakaba Endo, Noriko Togashi, Yasuko Kobayashi, Akira Onuma, Ryo Funayama, Matsuyuki Shirota, Keiko Nakayama, Yoko Aoki, Shigeo Kure |
Effect of structured weight bearing exercise on bone mineral density in children with Cerebral Palsy- an observational cohort | |
Ayush Gupta, U Singh, Biswaroop Chakrabarty, Prashant Jauhari, Atin Kumar, Manisha Jana, P Chaturvedi, Vandana Jain, R M Pandey, Sheffali Gulati |
Which is the most common physiological type of Cerebral Palsy in India? | |
Mayank Vrujlal Detroja, Mahesh Kamate |
General Movement Assessment in High Risk Infants in Sri Lanka: Experience from a Large Tertiary Care Hospital | |
gemunu prabhath hewawitharana, Piyumi Sasikala Wickramarachchi, Ayesha Yaddehi, R.D. Susantha Kumara, K.V. Kanchana Nilukshika, K.M.I. Induli, D.R. Sadeepi Chathuranga, D.L.N. Priyangika, W.R.A. Shantha, Sajee Anuradha Gamage, Bimba D.R. Hewawitharana, Champa J Wijesinghe |
Association of comorbidities in cerebral palsy with GMFCS, CP type and Quality of life : An observational study at a tertiary care hospital | |
JAYANTI PRABHA, areesha alam, Rashmi Kumar, Chandrakanta kumar, neera kohli |
Assessment of Neurodevelopmental Status in Infants and Children with Neonatal Hypoglycemic Brain Injury –characterise the Spectrum of Neurodisability (6-42 months)- Pilot Study | |
pradnya gadgil, Vidhi Shah, Shailee Shah, Abhishek Srivastava |
Neurodevelopmental assessment of children and adolescents with Neonatal Hypoglycemic Brain Injury (NHBI) to establish the developmental profile in the age group of 6 years- 16 years: A Pilot Study | |
pradnya gadgil, Yuvika Kamdar, Pavitra Desai, Abhishek Srivastava |
NEURO-DEVELOPMENTAL DELAY AND MALNUTRITION IN CHILDREN 0-6 YEARS IN MARGINALIZED RURAL INDIA | |
nandita chattopadhyay |
Motor outcome after Therapeutic Hypothermia in infants with Hypoxic-Ischaemic Encephalopathy | |
Marieke Kuiper, Linda Meiners, Elizabeth Chandler, Rick Brandsma, Arend Bos, Hendrik ter Horst, Deborah Sival |
Association of interleukin -6 Polymorphism and mRNA expression in cerebral palsy – a Pilot study | |
Anju Aggarwal, Sonali Verma, Anurupa Chakraborty, Neha Bansal, Shambhavi Roy |
Efficacy of Botulinum Toxin on Spasticity and Functional Outcome in Cerebral Palsy: an evaluation | |
Lokesh Lingappa |
A retrospective study to look for aetiology of cerebral palsy, time at diagnosis and the time taken to start rehabilitation services in patients following rehabilitation services at Lady Ridgeway Hospital, Colombo, Sri Lanka | |
Amali Dalpatadu, Samantha Waidyanatha, Pyara Ratnayaka, KCS Dalpatadu |
Solution to problem of Plenty | |
Rahul Bharat |
Home medical care for children with severe motor and mental disabilities | |
MARIKO MAEZAWA |
Gabapentin in the management of dystonia: an open labeled study | |
payal shah, vrajesh udani, Alita Misquitta |
Clinical course and seizure outcome of symptomatic epilepsy in cerebral palsy patients : community based study | |
Noha El tantawi, Dina Abd Elmegid |
Resting state cerebral glucose metabolism using [18]Fluoro-Deoxy-Glucose-Positron Emission Tomography (FDG-PET), Central Motor Conduction Times (CMCT) and Somatosensory Evoked Potentials (SEP) in children with dystonic cerebral palsy (CP) | |
Stavros Tsagkaris, Verity McClelland, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Keyoumars Ashkan, Richard Selway, Alexander Hammers, Jean-Pierre Lin |
Neonatal Hypoglycemic Brain Injury in the indian scenario : Risk Factors And Clinical Profile | |
payal shah, vrajesh udani, Neelu Desai |
ASSESSMENT OF IMPROVEMENT IN FUNCTIONAL ABILITY AND COMORBIDITIES OF A COHORT OF CHILDREN WITH CEREBRAL PALSY | |
PARVATHI MOHAN |
From cerebral palsy to hereditary spastic paraplegia: à propos of three patients | |
Dina Rose Amrom, Sara Seneca, Cedric Ballez, Monique Cordonnier, Peter De Jonghe, Jonathan Baets, Massimo Pandolfo, Julie Soblet, Guillaume Smits |
Clinical, radiological and genetic findings in a cohort of 60 polymicrogyria patients | |
Dina Rose Amrom, Annapurna Poduri, Nicolas Deconinck, Bernard Dan, Cynthia Prigogine, Anne Monier, Alec Aeby, Guillaume Smits, Emmanuel Scalais, Ingrid Unterberger, Eugen Trinka, François Dubeau, Donatella Tampieri, Jean-Claude Décarie, Jacques Michaud, Paul Mark, William B Dobyns, Christopher A Walsch, Frederick Andermann, Eva Andermann |
Mothers’ perception in changes of hand skills pattern of their children with cerebral palsy to perform activities of daily living in Bangladesh | |
Md. Yeasir Arafat Alve |
Integrative management of Cerebral palsy- Ayurveda (Indian traditional medicine) with Rehabilitative therapies | |
Lekshmi M K |
Using Telemedicine to improve Access to Specialty Care for Underserved Patients with Neurodevelopmental Disorders. | |
Deepa Unnikrishnan Menon |
CNS Infections
Neurodevelopment of 24 children born in Brazil with congenital Zika syndrome in 2015 - case series study | |
Lucas Victor Alves, Camila E Parede, Germanna V Silva, Maria Julia Gonçalves Mello, João Guilherme Bezerra Alves |
Congenital Zika syndrome and infatile spasms - case series study | |
Lucas Victor Alves, Maria Júlia Gonçalves Mello, Patrícia Bezerra, João Guilherme Bezerra Alves |
Perceptions and beliefs underpinning parents’ understanding about Neurocysticercosis among their children: A qualitative study | |
Endrakanti Mounika |
Changing face of Pediatric Neurotuberculosis. | |
Kritika Tiwari, Purva Keni Karnavat, Anaita Udwadia Hegde |
Chikungunya infection and Horner Syndrome: a case report | |
Lucas Victor Alves, Filipe Marinho Pinheiro Câmara, Mayara Batista Granhara, Alfredo Meneses Neto, João Guilherme Bezerra Alves |
Reducing Turnaround Time (TAT) in the diagnosis of bacterial meningitis: Direct CSF analysis by Mass Spectrometry | |
Varnit Shanker |
Should ionic calcium be a mandatory work up of suspected encephalitis | |
Varnit Shanker |
G-Therapy: A Hope For Patients With Subacute Sclerosing Panencephalitis! | |
Gunvant Devichand Oswal, Dr.Pooja Shrirang Upasani, Dr. Umesh D. Kalane, Dr.Nandan Yardi, Dr. Anaita Udwadia Hegde |
Clinico-Radiological Profile and Outcome of Children with Tubercular Meningitis in a Tertiary Care Centre in Bangladesh | |
Kanij Fatema, Kanij Fatema, Md Mizanur Rahman |
A case of mumps-related acute encephalopathy with biphasic seizures and late reduced diffusion | |
Takashi Shiihara |
Good Hearing Outcome in Children with non-polio Enteroviral Meningitis | |
Chew Thye Choong, Elis Lee, Henry Tan, Natalie Tan |
Should ionic calcium be a mandatory work up of suspected encephalitis | |
Varnit Shanker |
Seasonal Influenza-Related Neurologic Complications in Children from 2010 to 2015 | |
Eun Young Kim, Hui Jeong Yun, Hyung Min Cho |
Polymerase Chain Reaction of cerebrospinal fluid in children with acute bacterial meningitis | |
Rajniti Prasad |
A case of fulminant SSPE with transient EEG changes | |
Senthilkumar Vajramanickam |
Differentiating Scrub typhus meningoencephalitis from other Acute Encephalitis Syndrome In children in Uttar Pradesh, India | |
Pranshi Agarwal, Areesha Alam, Jayanti Prabha, Amita Jain, Chandrakanta Kumar, Sanjeev Kumar Verma, Rashmi Kumar |
Subacute Sclerosing Panencephalitis Presenting As Autoimmune Encephalitis | |
Ridhimaa Jain, Suvasini Sharma, Shilpa Devamare |
Clinical profile and outcomes in Acute Necrotising Encephalopathy Of Childhood: Case series from a tertiary care Pediatric centre in India | |
srikanth domala |
Rare case of streptococcus pneumoniae brain abscess in an infant | |
Surabhi Kaul, Rajan P Patel, Ian J Butler |
A new mouse model of congenital Zika virus infection reveals neurodevelopmental pathways disrupted in congenital Zika syndrome | |
Ganeshwaran Hitoshi Mochida, Tojo Nakayama, Amanda Guise, Kimino Fujimura, Anais Meziani, Long Cheng, Dylan Vaughan, Andrew Kodani, Ann Durbin, Irene Bosch, Mauro Teixeira, Hanno Steen, Lee Gehrke, Judith Steen |
A CASE SERIES OF EOSINOPHILIC MENINGITIS IN SOUTH INDIAN CHILDREN | |
sai chandar dudipala |
SUBACUTE SCLEROSING PANENCEPHALITIS IN POST-MEASLES VACCINATION ERA-THE CHANGING EPIDEMIOLOGICAL TRENDS AND NEED FOR EARLY VACCINATION | |
EKTA AGARWAL, Dr. Kavita Srivastav, Dr. Surekha Rajadhyaksha |
Atypical CNS infection: needs a mention. | |
abhijeet vilas botre |
AUTOIMMUNE ENCEPHALITIS, AN EASILY OVERLOOKED ENTITY | |
Fadila Sufyan |
Perceptions and beliefs underpinning parents’ understanding about Neurocysticercosis among their children: A qualitative study | |
Endrakanti Mounika |
Congenital CMV infection- A rare cause of Central Diabetes Insipidus | |
Ambrin Akhtar |
Japanese Encephalitis with Neurocysticercosis- Coexistence or Coincidence | |
MAROTI KADAM, Rajwanti K Vaswani, Shagun Shah, Baliram Gore, Chandrahas T Deshmukh, Jane David |
Meningitis in patients with cerebral palsy: a review of eighteen cases from a single institution | |
Varnit Shanker |
Treatment outcome of children with Congenital CMV infection at ICH and Dr. MR Khan Shishu(Children) Hospital | |
MASHAYA ZAMAN KOLI, SELINA HUSNA BANU, RAWNAK ARA |
Cytokine and chemokine responses in clinically mild encephalitis/encephalopathy with a reversible splenial lesion (MERS) by type | |
Shinichiro Morichi |
A case series of CNS influenza (H1N1) infection. | |
abhijeet vilas botre |
ANALYSIS OF 126 CASES OF “ACTUTE ENCEPHALITIS SYNDROME” IN A PEDIATRIC ICU. | |
Ramakant Sabharwal, Praveen Kumar, SUMIT BHOJWANI, Sapna jain |
Clinico-epidemiological profile and outcome of pediatric neurotuberculosis: a retrospective cohort study | |
Biswaroop Chakrabarty, Vivek Sirolia, Mudit Aggarwal, Prashant Jauhari, Atin Kumar, Sheffali Gulati |
complete remission of a case of SSPE with intrathecal interferon alpha. | |
Nirendra Kumar Rai, ruchi singh |
BILATERAL STRIATAL BRAIN ABSCESS- A RARE SITE, A RARE ORGANISM | |
Srinivasavaradan Govindarajan, INDRABHUSHAN SINGH, KANIKA GOYAL, ARUSHI GAHLOT SAINI, RENU SUTHAR, SAMEER VYAS, JAYASHREE MURALIDHARAN, MEENU SINGH |
Clinical Outcome at 18 months following Acute Flaccid Myelitis due to Enterovirus D68 | |
Jay Shetty, Lauren Marie Smith, Jacqueline McPherson, Paul Eunson, Kenneth McWilliam, Catherine McDougall, Kate Templeton |
YIELD OF GENEXPERT AND OUTCOMES IN PEDIATRIC TUBERCULAR MENINGITIS | |
Lokesh Lingappa |
High burden of neurological presentations in children admitted to Kenyan hospitals: A multi-hospital cohort study. | |
Jane Hassell, Thomas Julius, Morris Ogero, Charles RJC Newton, Mike English, Sam Akech |
Enterovirus-D68 associated acute flaccid myelitis in Europe- Clinical and epidemiological data from European Collaboration | |
Jay Shetty, Marjolein Knoester, Jelte Helfferich, Oebele Brouwer, Coretta Van Leer-Buter, Randy Poelman, Hubert Niesters, EU EV D68 Working Group |
A prospective cohort study to assess seizure recurrences in children with calcified neurocysticercosis | |
Abhijit Modak, Renu Suthar, Jitendra Kumar Sahu, Naveen Sankhyan, Niranjan Khandelwal |
SSPE mimicking anti-NMDA receptor encephalitis | |
Shilpa Devamare, Vikram Bhaskar, Himani Bhasin, Suvasini Sharma |
Syndromic Evaluations of CNS Infections by Multiplexed PCR Panels Enable Rapid Detection and Treatment of Infections | |
Siddhesh Chorghe, Sumir Pandit, Ashwini Chawathe, Pooja Gowda, Aparna Kotekar |
Brachial neuritis and Prolonged Survival: The Enigma of Rabies encephalomyelitis | |
Kanika Goel, Chandana Bhagwat, Arushi Gahlot Saini, Renu Suthar, Reeta Mani, Paramjeet Singh, Namita Ravikumar, Meenu Singh |
A prospective cohort study to assess seizure recurrences in children with calcified neurocysticercosis | |
Abhijit Modak, Renu Suthar, Jitendra Kumar Sahu, Naveen Sankhyan, Niranjan Khandelwal |
Post infectious Opsoclonus Myoclonus Ataxia Syndrome in Tropics | |
Sumeet Dhawan, Lokesh Saini, Prabhudev M Hiremath, Bhanudeep singanamala, Arundhati Mukherjee, Sameer Vyas, Jitendra Sahu, Jayashree M, Naveen Sankhyan |
What is the optimal duration of Anti-convulsant therapy for Acute Symptomatic Seizures in Children with Acute Encephalitis Syndrome? | |
Sumeet Rajendra Dhawan, Jitendra Kumar Sahu, Pratibha Singhi, Naveen Sankhyan, Jayashree Murlidharan |
ENTEROVIRUSES NEUROINFECTIONS IN CHILDREN IN UZBEKISTAN. | |
Abrorjon Khoshimov |
Enzymatic changes in the CSF in children with neuroinfections in uzbekistan. | |
Makhmudjon Bakhromov |
Herpes encephalitis at children in Uzbekistan. | |
Makhmudjon Bakhromov |
Education and Training
PEDIATRIC NEUROLOGY SERVICES IN RURAL MAHARASHTRA, INDIA AN 8 YEAR TREND | |
Anaita Udwadia Hegde, Roshan Kore, Purva Keni Karnavat, Asha Chitnis, Snehal Deshpande, Chetna Bhatt, Gayatri Hattiangadi, Nitin Nirmal, Sachin Pingale |
The Quality of Life (QoL) in Indian Children with Learning Disorders – a case control study | |
lekha mishra |
Closing the Epilepsy Treatment Gap: A Pediatric Epilepsy Education Initiative for Primary Care Providers in Zambia | |
Leah Wibecan, Ornella Ciccone, Owen Tembo, Prisca Kalyelye, Manoj Mathews, Archana A. Patel |
Worldwide short course education programmes in epilepsy for paediatricians – are they effective? | |
Alison Gifford, Jo Wilmshurst, Finbar O'Callaghan, Mike Griffiths, Colin Dunkley, Philippa Rodie, Helen Cross, Martin Kirkpatrick |
Flipped classroom versus traditional lecture in training undergraduate medical students on pediatric epilepsy: A randomized controlled trial | |
Jaya Shankar Kaushik, Vandana Arya, Radhamohan Rana, Anjali Verma, Harish Bhardwaj |
Experience in providing a short training on EEG recording technique and reviewing in Bangladesh, Tanzania and Ghana | |
SELINA HUSNA BANU, Naila Zaman KHAN |
Development Cognition and Psychiatry
Gratification phenomena in infancy: a report of twenty-nine children. | |
ROSHAN KOUL |
Predictors of intellectual abilities among children with autism spectrum disorder | |
Watfa Al-Mamari, Ahmed Babiker Idris, Ahlam Ali Abdelsattar, Abeer Al-Mujaini, Muna Al-Jabri |
The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India | |
shriganesh patil, Abhinav Neela, Arpita Thakker, Smita Patil, Nandkishor Jadhav, Mona Gajre |
The Assessment and Management of Childhood Masturbation: An Analysis of 45 Cases | |
Hüseyin Per |
Near-infrared spectroscopy (NIRS) based neurofeedback training in children with Tourette syndrome(TS) | |
Pou-Leng Cheong, Chia-Wei Sun |
ROLE OF LINGUISTIC PROFILING INASSESSMENTS OF LEARNING AND LANGUAGE DISORDERS IN INDIAN CHILDREN-A CASE CONTROL STUDY | |
MsNitya Raman, Dr Mona Gajre, DrNandini Singh |
A NON LINEAR DYNAMIC AYURVEDA APPROACH FOR THE MANAGEMENT OF CHILDREN WITH AUTISM SPECTRUM DISORDER | |
DINESH KS, RAJESH N, JAYADEVAN CV, GEORGE MJ, ANITA PATEL |
The sensory processing patterns of children with Autism Spectrum Disorder: Impact on behavior problems and adaptive behavior | |
MUTHUVEL RAJANGAM |
To test if separation anxiety(SA) is absent/attenuated in autistic children | |
Nisreen Hussain Bohra |
The Quality of Life (QoL) in Indian Children with Learning Disorders – a case control study | |
lekha mishra, jagruti bawa, smita patil, arpita thakker, manikantan r, mona gajre |
Tuberous Sclerosis Complex (TSC)-Associated Neuropsychiatric Disorders (TAND): New Findings on Age, Gender and Genotype in Relation to Intellectual Phenotype | |
Petrus J De Vries, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D´Amato, Guillaume B d'Augères, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Rima Nabbout, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C Kingswood, Anna C Jansen |
The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India | |
shriganesh patil |
The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India | |
shriganesh patil, Abhinav Neela, Arpita Thakker |
PROFILE OF CHILDREN WITH AUTISTIC SPECTRUM DISORDER ATTENDING A PUBLIC HEALTH HOSPITAL-AN INDIA EXPERIENCE | |
Dr Vidya Manjeri, Ms preeti Gurav, Ms Bhakti Anant Vanmali, Dr Sushant Sarang, Dr Avinash Dsouza, Dr Mona P Gajre |
A STUDY ON HEAVY METALS PROFILE IN CHILDREN WITH AUTISM | |
Mogili Sudha Priyanka, SAVITA VERMA ATTRI, PRATIBHA SINGHI, PRAHBHJOT MALHI, JITENDRA KUMAR SAHU, ARUSHI GAHLOT SAINI |
Creating an assessment scale of social and behavioral development for preschool children -The process of creating the scale- | |
Hideyo Goma, Shun Tanaka, Michio Ushiyama, Tomomi Ikeda, Rika Ochiai, Toshihiro Kato, Satomi Shimizu, Kazuhisa Inoue, Reiko Ushio, Hiromi Kotani |
Cognitive visual dysfunctions in children with autism spectrum disorders and other developmental disabilities | |
Eu Gene Park, Young Hoon Kim |
“Prevalence of Autism spectrum disorders (ASD) in a latinamerican city, first epidemilogical study in children 18 – 36 months of age” | |
Francisco Alberto Astorino, Elena Carrera, Liliana Contini |
Effect of a Combination of Carnitine, Coenzyme Q10 and Alpha-Lipoic Acid (MitoCocktail) on Mitochondrial Function and Neurobehavioral Performance in Children with Autism Spectrum Disorder | |
Agustin Legido, Michael Goldenthal, Brigid Garvin, Shirish Damle, Kelleen Corrigan, James Connell, Diana Thao, Ignacio Valencia, Joseph Melvin, Divya Subramanian Khurana, Mitzie Grant, Craig Newschaffer |
PREVALENCE AND CLINICAL CHARACTERISTICS OF AUTISM SPECTRUM DISORDER AT A TERTIARY HOSPITAL IN ZAMBIA | |
Kafula Lisa Nkole, Ornella Ciccone |
The Effect of Glucocorticoid Receptor (GR) Function on the Behavior of ADHD Rats and the Mechanism of Interaction between GR and MAO A | |
Yanhui Chen, Hongzhu Lu, Jun Hu, Xiaoxia Lin |
Neurodevelopmental Outcome After Neonatal Hypoglycemic Brain Injury . | |
Madhavi Shelke, Abhay Jain, Madhura Anvikar, Pratima weldode, Abdul Muqueet |
Parental use of rehabilitation services and complementary therapy for autism in Jordan | |
amira masri |
ROLE OF LINGUISTIC PROFILING INASSESSMENTS OF LEARNING AND LANGUAGE DISORDERS IN INDIAN CHILDREN-A CASE CONTROL STUDY | |
Nitya Raman, MONA GAJRE, DrNandini Singh |
The prevalence of parental ADHD in children newly diagnosed with ADHD in urban India | |
shriganesh patil, Abhinav Neela, Arpita Thakker, Smita Patil, Nandkishor Jadhav, Mona Gajre |
Tele medicine via Video Consultations for children awaiting Developmental Assessement | |
Edith Posener |
All work and no play: The relationship of leisure time activities and psychological disorders in school children | |
Pallavi Bhad, Gouri Rao Passi |
Vitamin B12 status and Neurodevelopmental delay in Infants in Northern India | |
Chandrika Azad |
Eating behaviour in Children with Autism | |
Sachitra Rathod, Subramanian Mahadevan |
Plasma amino acid profile in children with autism spectrum disorder | |
Wen-Xiong Chen, Min-Zhi PENG, Yan-Na CAI, Zhi-Fang HUANG, Jin-Yu HUANG, Si-Yuan YANG, Peng YI, Li LIU |
Acupuncture for non-verbal autistic children: a randomized controlled trial | |
Wen-Xiong Chen, Gang LIU, Hong-Sheng LIU, Zhi-Fang HUANG, Jin-Yu HUANG, Si-Yuan YANG |
18 F- FDG PET scan abnormalities at rest in children with Autism Spectrum Disorder | |
Razia A Kadwa, Pratibha D Singhi, Prahbhjot Malhi, Jitendra K Sahu, Naveen Sankhyan, Mittal B.R, Rajinder K |
Pseudospasticity dysbasya in children | |
Julia Sadovskaya, Valentina Rodionova, Maria Karpilova, Anna Bitova |
The Clinical Profile of epilepsy and electroencephalographic abnormalities in Children with Autistic Spectrum Disorder – A Retrospective Study | |
ALPANA SANTOSH KONDEKAR, Sandeep Bavdekar |
PSYCHIATRIC CO-MORBIDITIES IN CHILDREN WITH AUTISM SPECTRUM DISORDERS | |
Somini Haresh Mehta, Neelu Desai |
Efficacy of Weighted Compression Vest on Hyperactivity, Inattention and Core Symptoms in children with Autism Spectrum Disorder: an interventional pilot study | |
Nishtha Gupta, Deepti Gupta, Aparajita Gupta, Shobha Sharma, Lokesh Saini, Prateek Kumar Panda, Asha Chitnise, Sheffali Gulati |
Health related Quality of Life in Children with Autism Spectrum Disorder aged 3-12 years and correlation with severity of autism and behavioral co-morbidities: a cross-sectional study | |
Prateek Kumar Panda, Sheffali Gulati, Sanjeeda Khan, Shobha Sharma, Priyanka Madaan, Bhavya G, Prashant Jauhari, R M Pandey |
Spectrum of Genetic Etiologies in children with Autism Spectrum Disorder: a single institution observational study | |
Sheffali Gulati, Prateek Kumar Panda, Priyanka Madaan, Prashant Jauhari, Biswaroop Chakrabarty, Aparajita Gupta, Ankita Pal, Sachendra Badal, Vishal Sondhi, Neerja Gupta, Madhulika Kabra |
A Mobile Autism Risk Initiative (AMARI) to Detect Autism Spectrum Disorder in Bangladeshi Children Under the Age of 4 | |
Dennis P Wall |
Analysis of outcomes of an interdisciplinary developmental program for syndromic children with neurological deficits | |
DIPTI KHOPKAR, SAMIR DALWAI |
Neurodevelopmental disease pattern in a tertiary care hospital-An experience in Bangladesh. | |
BISWAJIT CHOWDHURY |
Comparison of blood heavy metal levels in children with Autism Spectrum Disorder aged 3-12 years and typically developing children: A cross sectional study | |
Sheffali Gulati, Aparajita Gupta, Shobha Sharma, Prateek Kumar Panda, Biswaroop Chakrabarty, Rachna Sehgal, Amita Srivastava, Y K Gupta, R M Pandey |
Comparison of Executive Function between children with Autism Spectrum Disorder and Typically Developing Children: a Cross-sectional study | |
Ratna Sharma, Asfa Ahmad, Shobha Sharma, Prateek Kumar Panda, Aparajita Gupta, Rupesh Samanchi, Sana Sayeed, Prashant Jauhari, Biswaroop Chakrabarty, Sheffali Gulati |
Nutritional Status of Children with Autistic Spectrum Disorder | |
Dr. Vidya Manjeri, Priya Karkera, Disha Bagadia, Bhakti Anant Vanmali, Dr. Sushant Sarang, Dr. Avinash Dsouza, Dr. Mona P. Gajre |
Clinical Spectrum and Management Outcome of Psychogenic Non Epileptic Seizures in Children: A Prospective Observational Study | |
Sheffali Gulati, Shobha Sharma, Prateek Kumar Panda, Priyanka Madaan, Prashant Jauhari, Biswaroop Chakrabarty |
Cognitive Functioning in Children with Epilepsy: Generalized Seizures (GS), Complex Partial Seizure (CPS) and Temporal Lobe Epilepsy (TLE) | |
Gopukumar Kumarpillai, Sree Krupa Manthri, ashwini S Kalkunte, Umashankar R, shobha Nandavar, Girish Gadre, Murthi G |
NON PHARMACOLOGICAL PROTOCOL FOR TREATING ADHD CHILDREN (NFB,CES,CCT) | |
hussein hosny abdeldayem |
Mobile Media Use in Children with a Neurodevelopmental Disorder from the ages of 0-8years. | |
Franzina Coutinho, Akansha Shah, Shantanu Tilak, Neelu Desai, Vrajesh Udani |
Use Of mobile media among children (0-8years) with ASD against the typically developing control group | |
Franzina Coutinho, Akansha Shah, Shantanu Tilak, Neelu Desai, Vrajesh Udani |
Prevalence of internet gaming disorder in patients in the age group 5-12 years presenting to the outpatient department of a tertiary care hospital in Delhi | |
Meenakshi Bhatt, Rachna Sehgal, Aditi Tiwari |
Can specific EEG criteria contribute as a neural marker for the siblings of Autistic children? | |
Razia Sultana |
NEUROCOGNTIVE OUTCOMES IN SURVIVORS OF CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA | |
Vishwa CR, Rachna Seth |
The Perturbance of Microbiome and Gut Brain Axis in Autism Spectrum Disorders | |
Sue Xue Ming |
INFLUENCE OF SENSORY INTEGRATION OCCUPATIONAL THERAPY IN REDUCING NEGATIVE BEHAVIOR 2 TO 5 YEARS CHILDREN WITH AUTISM SPECTRUM DISORDERS | |
Junita Elvira, Hardiono D Pusponegoro, Setyo Handryastuti |
Rare diseases presenting with Autism Spectrum Disorder (ASD); An etiological conundrum | |
Vrushabh Sopan Gavali, Leena Srivastava, Nirali Thakker, Sujit Jagtap |
Association between Sleep Disturbances and Sensory-over-responsivity in Children with Autism Spectrum Disorder. | |
Akansha Shah, Somini Mehta, Neelu Desai, Vrajesh udani |
A Study of Trace Elements Status in Children with Infantile Tremor Syndrome: An Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) Based Study | |
Trinity Deepak Francis |
EVALUATION OF HYPERANDROGENISM IN CHILDREN WITH AUTISM SPECTRUM DISORDER AND AGE-SEX MATCHED CONTROLS | |
Neeharika Sriram |
EVALUATION OF HYPERANDROGENISM IN CHILDREN WITH AUTISM SPECTRUM DISORDER AND AGE-SEX MATCHED CONTROLS | |
Neeharika Sriram, Jitendra Kumar Sahu |
Children's Pathology Leading to Disruption of Object Relations | |
Umesh Jain |
The effect of omitting breakfast on cognitive function and blood glucose level among adolescent secondary school students | |
Halima Adamu |
Targeted gene sequencing in children with autism spectrum disorder | |
Mary Iype, Anitha Ayyappan, PA SURESH |
AUTISM - Is there an increased risk from ART (artificial reproductive technique) | |
Darshana N Vora, Nitish S Vora |
Demographic details of children with Autism presenting to a specialist Autism center | |
Darshana N Vora, Nitish S Vora |
Early Detection of Developmental Problems by Parents | |
Sundara sabaratnam Sam LINGAM |
Diagnostic Investigations of Children with Learning Difficulties | |
Sundara sabaratnam Sam LINGAM |
Magnitude of sleep problem in children with Neurological disorders compared with normal population | |
Darshana N Vora, Nitish S Vora |
Cranial neuroimaging findings in nutritional vitamin B12 deficiency (NVBD) in infants | |
Jatinder Singh Goraya |
Picky Eating in Autism Spectrum Disorder, its Characters and Treatment | |
Shigeru Hanaoka |
Autism and ADHD: Differential functioning on a Computerized Performance Test (MOXO-CPT) | |
YAEL LEITNER |
STRUCTURE OF SLEEP IN CHILDREN WITH EPILEPSY AND COGNITIVE IMPAIRMENT. | |
Abrorjon Khoshimov |
Shared atypical functional connectivity in children with autism spectrum disorder and attention- deficit/hyperactivity disorder | |
EVDOKIA ANAGNOSTOU |
A Phase 2 Randomized, Placebo-Controlled Trial of Tideglusib, an Orally Administered GSK3Beta Inhibitor, in the Treatment of Adolescents with Autism Spectrum Disorder | |
EVDOKIA ANAGNOSTOU |
Epilepsy
Evaluation of vitamin B12 levels in children with Infantile spasms and children with Global Developmental Delay without Infantile spasms: A cross sectional observational study | |
Mahender Kumar Meena |
EEG services for children in Africa: Pilot survey of capacity and needs | |
Veena Kander |
Febrile Infection Related Epilepsy Syndrome (FIRES) - A multi-centric study from India | |
Sandeep Bhagwan Patil, Neha Manjhani, Rakhi Sharma, Ravi Sharma, KP Vinayan, Arun Grace Roy, Vivek Jain |
Practical aspects of the use of Ketogenic Diet in the management of Childhood Epilepsy- a review of experience from Scotland | |
Elma Stephen, Lucy Elphinstone, Helen Grossi, Tracy Cameron |
Efficacy of Modified Atkins Diet (MAD) as Treatment for Intractable Epilepsy in Children - A Randomized Controlled Trial. | |
Nazmul Haque |
Assessment of Oral Hygiene of Children with Epilepsy | |
Mohammed M Jan |
Clinical Profile and Outcomes of Epilepsy surgery in children from tertiary epilepsy care center India | |
Sandeep Bhagwan Patil, Nilesh Kurwale, Sujit Jagtap |
Treatment approach for neonates with acute symptomatic seizures influences length of hospital stay | |
Hannah C. Glass |
Levels of Immunoglobulins, Complement and T Lymphocyte Subsets in the Peripheral Blood of Children with Convulsive Diseases and Their Signifiances | |
XY GUO |
Plasma Galanin and Neuropeptide Y Levels in Children with Convulsive Diseases and Their Signifiances | |
XY GUO |
Classifying Electroencephalographic Diagnoses of Epilepsy without Epileptiform Discharges and Nonepileptic Paroxysmal Events Using Deep Convolutional Neural Networks | |
Lung-Chang Lin, Chen-Sen Ouyang, Ching-Tai Chiang, Rong-Ching Wu, Hui-Chuan Wu, Rei-Cheng Yang |
The clinical efficacy and follow-up study of ketogenic diet adding treatment for refractor epilepsy in children | |
Zeshu Ning |
TITLE: PAROXYSMAL NON-EPILEPTIC EVENTS IN A PEDIATRIC EPILEPSY CLINIC: A PROSPECTIVE STUDY | |
Neelu desai |
The latest finding of genetic testing in Chinese patients with unexplained Epileptic encephalopathy(EE) | |
Sun Dan |
Canonical transient receptor potential chan nel 3 contributes to recurrent febrile seizure s by inducing neuronal cell death and neuroi nflammation | |
Sun Dan |
Study of 15 patients with early infantile epileptic encephalopathy -treatable Neurometabolic causes | |
harshuti biren shah |
Factors associated with Electroencephalographic and Clinical Remission of Benign Childhood Epilepsy with Centrotemporal Spikes | |
Su Jeong You, Eun Hye Lee |
GABA TRANSAMINASE DEFICIENCY DISORDER IN AN INDIAN FAMILY - REPORT OF TWO NEW CASES | |
Ruchita Vyas, Omkar Hajirnis, Purva Keni Karnavat, Anaita Udwadia Hegde |
KETOGENIC DIET: DO WE NEED 4:1 RATIO FOR KETOSIS? | |
Purva Keni Karnavat, Anaita Udwadia Hegde, Shilpa Kulkarni, Roshan Kore, Bhakti Tulaskar, Suvarna Sawant |
Epilepsy Genetics – a new weapon in our Armamentarium! | |
Dr Tarishi Nemani, Dr Vishal Kanubhai Patel, Dr Purva Keni Karnavat, Dr Anaita Udwadia Hegde |
Clinical features and efficiency of ketogenic diet of 106 Dravet syndrome patients | |
JING PENG |
Analysis of clinical and genetic features of 30 patients with KCNQ2-related disorder | |
JING PENG |
CLINICO-ETIOLOGICAL PROFILE OF REFRACTORY STATUS EPILEPTICUS IN CHILDREN | |
KC Sadik, Devendra Mishra, Urmila Jhamb, Monica Juneja |
Electroencephalogram Features of Children with Type 1 Diabetes Mellitus | |
Ceren Gunbey, Ruken Yıldırım |
Perampanel and Brivaracetam: Efficacy and safety in pediatric refractory epilepsy | |
Divya Subramanian Khurana, Ana Melikishvili, Sara McGuire, Karen S Carvalho, Ignacio Valencia, Daphne M Hasbani, Uzma Sharif, Agustin Legido |
Intravenous Fosphenytoin loading dose of 20 mg/kg in Status epilepticus: Is it enough in Indian children? | |
Kavita Srivastava |
It’s not all about seizures: Experience of Dravet Syndrome management in a Scottish Children’s Hospital | |
Sylvia Yuk San Tran, Elma Stephen |
First Complex Febrile Seizure – do we need to investigate. | |
Arpita Devbrata Adhikari, Krishna Shetye, Smita Patil, Mona Gajre |
Prevalence of Epilepsy and Inter-ictal Epileptiform discharges in children with Neurodevelopmental disorders | |
B Anukirthiga, Devendra Mishra, Sanjay Pandey, Monica Juneja |
Seizures in children with Zika Virus Congenital Syndrome | |
Lucas Victor Alves, Patrícia Gomes de Matos Bezerra, Maria Júlia Gonçalves de Mello, Ana Rodrigues Falbo, José Natal Figueiroa |
A critical analysis of lumbar puncture in the emergency management of febrile seizures: a cross-sectional study | |
Eduardo Jorge da Fonseca Lima, Gabriel Brito de Moura Monteiro, Alberto de Barros Lima Filho, Lucas Victor Alves |
Clinico-etiological Profile and Developmental Status of Infants Aged 1-24 months with Epilepsy in India | |
Pankaj Kumar Sahu, Devendra Mishra, Monica Juneja |
Ohtahara Syndrome due to unique Heterozygous PIGO mutation: Clinical and EEG features | |
Arayamparambil C Anilkumar |
Congenital Mirror Movements with epilepsy in association with KCNT1 gene mutation: A Case Report. | |
RAGHAVENDRA K |
National Surveillance of Mortality in Children with Epilepsy in the UK and Ireland | |
Omar Abdel-mannan, Alastair Sutcliffe |
The absence of NIPA2 enhances neural excitability through BK channels | |
Han Xie, Nana Liu, Wenshu Xiangwei, Kai Gao, Tianshuang Wang, Yuwu Jiang |
Pediatric status epilepticus. Cases admitted during years 2015-2016 at Hospital de niños Dr. O. Alassia de la ciudad de Santa Fe, Argentina. | |
Francisco Alberto Astorino, Betiana Comas, María Inés Malatini |
Efficacy of adjunctive vagus nerve stimulation in patients with Dravet syndrome | |
Songee Youn |
Evolution of epileptic zeisures iniciated during neonatal period in a long term follow up of 97 children | |
Francisco Alberto Astorino, María Ines Malatini, Betiana Comas |
Febril status epilepticus in children. Series of cases of children admited at Dr. O Alassia Hospital, Santa Fe Argentina period 2015 to 2018 | |
Francisco Alberto Astorino, Betiana Comas, María Inés Malatini |
Absence epilepsy, the great masquerader | |
Samata Singhi |
Not all that blinks is tics | |
Samata Singhi |
Epileptic Spasms in Southern Africa | |
Sharika V Raga |
Autoimmunity of childhood epilepsy | |
sonali verma, Anju Aggarwal, Gargi Rai, Shukla Das |
KETOGENIC DIET IN ZAMBIA: MANAGING REFRACTORY EPILEPSY IN A LOW INCOME COUNTRY. | |
Kafula Lisa Nkole, Nfwama Kawatu, Chimbizyani Kanyinji, Theresa Njobvu, Ornella Ciccone, Stacey Tarrant, Archana A Patel, Annmarie Bergin |
Open label randomized comparison of levetiracetam and sodium valproate monotherapy in childhood epilepsy | |
SWATI BHAYANA |
Hemimegalencephaly with congenital facial lipoma-A Case Report | |
Subramanian Velusamy, Subramanian Velusamy, Balaraman Krishnakumar |
The efficacy and safety of levetiracetam treating in pediatric epilepsy in different ages and seizure types | |
Yu Liu, Xueying Wang, Gaobo Ye, Shaoping Huang, Lin Yang |
A Chinese boy with Malonyl-CoA decarboxylase deficiency and a novel mutation in the MLYCD gene | |
Fang Wang, Lin Yang |
Nurse Lead “Multi Levels” Pediatric Epilepsy Education Initiatives | |
Amal Chaman Chehab |
Experience with very high dose (8mg/kg/day, maximum 60mg/day) prednisolone for West syndrome in a resource limited setting | |
Sunil Malik |
Comparison Of Electroencephalographic Sleep Stages With Bispectral İndex Data İn Children | |
Sanem Yılmaz, Hasan Tekgul, Erdem Simsek, Hande Tekin, Hepsen Mine SERIN, Gul Aktan, Sarenur Gokben |
Effects of ketogenic diet on plasma levels of valproic acid in children with epilepsy | |
Fang Wang, Jinqiu Wang, Baoni Mu, Lin Yang |
Cannabinoid receptor type 2 controls neuronal autophagy through regulation of mTOR signal pathway during the repair of hippocampal neurons in status epilepticus rats | |
Qiong Wu, Hua Wang |
Comparison of Epileptic Seizure Classifications (ILAE-1981 and ILAE-2017) with A Modular Education Program Among Residents in Pediatrics | |
Meherrem Imanli, Hasan Tekgul, Erdem Simsek, Hepsen Mine Serin, Seda Kanmaz, Sanem Yilmaz, Gul Aktan, Sarenur Gokben |
Tuberous Sclerosis Complex (TSC) - Associated Epilepsy: Final Results from the TOSCA Study | |
Rima Nabbout, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D´Amato, Guillaume B d'Augères, Petrus J De Vries, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, Anna C Jansen, John C Kingswood |
Perampanel in paediatric population: experience in a regional hospital | |
Nikole Ada Tracy, Wing Cheong Lee, Li Yan Tsung, Shuk Mui Tai, Kam Tim Liu |
Risk Of Recurrence After Withdrawal Of Antiepileptic Medication In Children With Epilepsy | |
Mizanur Rahman, Sufia Khatun Sumi, Kanij Fatema |
WWOX related epileptic encephalopathy: A new autosomal recessively inherited disorder | |
Hepsen Mine SERIN, Gurkan Gurbuz, Betul Kilic, Bulent Kara, Sarenur Gokben |
Analysis of curative effect and influence factors of small dose and short course of ACTH on 73 cases of IS | |
Xiaodi Han, Fang Fang, Chunhong Chen |
Clinical and EEG characteristics of epilepsy of infancy with migrating focal seizures | |
Shuqian Zhang, Ruopeng Sun, Baomin Li |
De novo Mutation among a Chinese Infantile Spasms Cohort and Precision Treatment with Levetiracetam in Four de novo STXBP1 Mutation Patients | |
Li-ying Liu, Fang Liu, Yang-yang Wang, Gui-Xia Zhang, Meng-Na Zhang, Qian Lu, Li-Ping Zou, Xiao-Li Chen |
The value of mobile phone videos in increasing the diagnosis accuracy and saving cost of consultation for infant paroxysmal events: a prospective study in China | |
Lu-Lu Huang, Yang-Yang Wang, Li-Ying Liu, Hong-Ping Tang, Meng-Na Zhang, Shu-Fang Ma, Li-Ping Zou |
Establishment and utility assessment of Posterior Reversible Encephalopathy Syndrome early warning scoring (PEWS) scale Establishment and utility assessment of PEWS scale | |
Li-Ping Zou, Hui Li, Li-ying Liu, Yang-yang Wang, Ying Liu, Jing Chen, Lin-Yan Hu, Meng-Jia Liu, Meng-Na Zhang, Shu-Fang Ma |
First unprovoked seizure in children-Predictors of recurrence | |
Smita Prabhakar Patil |
Clinical characteristics and genetic features of benign infantile epilepsy with PRRT2 mutation | |
ChunHong Chen, HuSheng Wu, XiaoHui Wang, HongMei Wang, XiaoTun Ren, JunLan Lv, Fang Fang |
Adverse drug reactions of anti-epileptics in children-an observational studySundeep Kaushik, Suvasini Sharma, Deepti Chopra, Bijoy Patra, Satinder Aneja | |
Dr Sundeep Kaushik |
The latest finding of genetic testing in Chinese patients with unexplained Epileptic encephalopathy(EE). | |
Liu Zhi Sheng |
A unique variant of West Syndrome:Vitamin B12 responsive epileptic encephalopathy | |
Harshkumar Arvindbhai Patel, Prarthana Kharod, Prarthana Kharod |
Clinical profile and short-term outcome of status epilepticus in children | |
Chinmay Chetan, Satinder Aneja, Suvasini Sharma, Bijoy Patra, Surendra Bahadur Mathur |
Accelerated corticospinal tract maturation, as measured by neuronavigated transcranial magnetic stimulation (nTMS), corresponds to preserved IQ in girls, but not in boys, with focal epilepsy | |
Harper Lee Kaye, Clemente Vega, Ali Jannati, Melanie McNally, Gabrielle Block, Alvaro Pascual-Leone, Alexander Rotenberg |
SYNDROMES AND ETIOLOGY IN PEDIATRIC EPILEPSY: EVALUATION OF INTERNATIONAL LEAGUE AGAINST EPILEPSY (ILAE) 1989, 2010 AND 2017 CLASSIFICATION OF EPILEPSY AT A TERTIARY CARE CENTRE IN INDIA | |
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, satinder aneja |
FEATURES OF EPILEPSY AND CEREBRAL PALSY IN CHILDREN IN UZBEKISTAN. | |
Abrorjon Khoshimov |
DESCRIPTIVE EPIDEMIOLOGY OF “CONTINUOUS SPIKE AND SLOW WAVE IN SLEEP (CSWS)” EPILEPSY AT A TERTIARY CARE CENTRE IN INDIA | |
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, Satinder Aneja |
Clinico-Etiological profile of acute seizures in children admitted in PICU and their short-term outcome | |
Suman Choudhary, DR SWATI MULYE, DR GUNJAN KELA MEHROTRA, DR CHANDAN KUMAR SHAW |
Profile of children with seizures and epilepsy presenting at a tertiary care specialist Paediatric epilepsy clinic | |
Nitish S Vora |
ELECTROCLINICAL PROFILES OF CHILDREN WITH BENIGN EPILEPSY WITH CENTROTEMPORAL SPIKES (BECTS) AT A TERTIARY CARE CENTRE | |
Aakanksha Anand, Suvasini Sharma, Bijoy Patra, Satinder Aneja |
Lacosamide responsive ESES (electrical status epilepticus in slow wave sleep )– 2 case reports | |
pradnya gadgil, Nilima Bhalerao, Sunita Venkatraman |
‘Prevent Neonatal hypoglycaemia, Prevent Infantile Spasms: Revealing findings from an etiological study on West Syndrome patients from North India | |
Prabhar Srivastava, Priyanka Surana, Romit Jain, Vedam Ramprasad, Thenral SG, Sakthivel Murugan, Vivek Jain |
A clinical and electrophysiological profile of epileptic spasms- A tertiary care centre experience | |
abhishek ravindra jain, mary iype, P A Mohammed Kunju, mini sreedharan, bindu thankappan |
A Practical Quality of Life Questionnaire for Children with Severe Intellectual Disability and Epilepsy: Comparing proxy reporting by Mothers and Fathers | |
Vivek Mundada, Deepak Parashar, APJ Parker |
Effectiveness and tolerability of perampanel in children under 7 years old with refractory epilepsy: A single-center, retrospective study | |
Fu-Man Chang, Wen-Chin Weng, Pi-Chuan Fan, Wang-Tso Lee |
A NEW VEGETATIVE SIGN RELATED TO ANTERIOR INSULA EPILEPSY: IPSILATERAL “GLOVE AND SOCK” SKIN CYANOSIS | |
Oana Tarta-Arsene, Oana Tarta-Arsene, Sergiu Stoica, Sergiu Stoica, Sorin Tarnoveanu, Diana Gabriela Barca, Sorin Tarnoveanu |
A case of KCNA2 encephalopathy presenting with various involuntary movements, severe psychomotor retardation, and sleep disturbance. | |
Tatsuharu Sato |
Infantile epilepsy with prolonged focal myoclonic seizures: A distinctive syndrome associated with TBC1D24 mutation. | |
Deepa Sirsi, John Schreiber, Satish Agadi, Robert S Greenwood, Susan T Arnold |
Status Epilepticus in Pediatric Patients Severity Score (STEPSS): A clinical score to predict the outcome of status epilepticus in children. | |
Sidharth Yadav, Suvasini Sharma, Bijoy Patra, Rajeev Malhotra, Virendra Kumar |
Screening for Mental Health Problems in Children and Young People with Epilepsy and Early Management in the Clinic Setting | |
Ailsa McLellan, Suzanne Felix, Catriona George, Kirsten Verity, Michelle Small, Celia Brand, Richard Chin, Jay Shetty |
What to expect from an unexpected seizure? | |
Rosa Lualdi, Giulia Bravar, Valentina Dolcemascolo, Paola Cogo, Giovanni Crichiutti |
THE CLINICAL CASE OF EPILEPTIC ENCEPHALOPATHY IN ANGELMAN SYNDROME. | |
Akmal Asatullayevic Mukhamedov |
Clinico-radiological and electrographic spectrum of children with Temporal lobe epilepsy: a retrospective cohort study | |
Zulfiqar Luhar, Biswaroop Chakrabarty, Ankita Pal, Prashant Jauhari, Atin Kumar, Shobha Sharma, Sheffali Gulati |
Outcome of Rasmussen Encephalitis with conservative management | |
Bijoy Patra, Surendra Bahadur Mathur, Kanti Lal Chakraborti, Preeti Gaddad, Suvasini Sharma, Satinder Aneja |
Clinical and Molecular profile of First Indian cohort of Unclassified West Syndrome Patients | |
Romit Jain, Priyanka Surana, Prabhar Srivastava, Thenral SG, Ramprasad V, Saktivel Murugan, Subathra Mahalingam, Aishwarya Subramaniyan, Sameer M Zuberi, Vivek Jain |
Microbiological diagnostic challenges in a seasonal cluster of Rhombencephalitis | |
smilu mohanlal, Lokesh lingappa, Ramesh Konanki, Nikit Milind Shah, Srikanth Domala, Ashwini Mohan, Ravi verma |
Achievement of camp in children with epilepsy | |
Monika Kukuruzovic, Masa Malenica, Iva Separovic, Kristna Kuznik |
ETIOLOGICAL CLASSIFICATION (ILAE-2017) AND THERAPEUTIC REPONSE IN CHILDREN WITH EPILEPSY PRESENTING AT A TERTIARY CARE SPECIALIST EPILEPSY CLINIC. | |
Nitish S Vora |
Hemiconvulsion Hemiplegia Epilepsy Syndrome: A case Report | |
DEEPAK DWIVEDI, Chitra soni, jyoti singh |
Prolonged Seizures in Children | |
Clodagh Mitchell, Jay Shetty, Libby Dickson, Celia Brand, Paul Leonard, Ailsa McLellan |
Study of Drug Resistant Epilepsy at a Tertiary Care Centre in Western India 2018 | |
Rasika Sandeep Bharaswadkar |
Pediatric lamotrigine overdose resulting in generalized seizure and encephalopathy | |
Djurdja Djordjevic |
Prevalence and association of risk factors for anticonvulsant polytherapy amongst epileptic children: A case-control study | |
Shifa Bidhan, Krishna M Adhikari, Rakesh Kumar Gupta |
Improving triaging of Infantile Spasm EEG referrals in a large Canadian institution | |
Djurdja Djordjevic |
A case of De Novo NAA10 mutation presenting with eyelid myoclonias (AKA Jeavons syndrome) | |
Vinod Valentine |
Parietal epilepsy presenting as eye flutter and absences | |
Kalyani Dilip Karkare |
Significance of polyspikes on electroencephalogram in children with focal epilepsy | |
Ara Ko, Ju Hyun Kong, Yun-Jin Lee, Sang Ook Nam |
Experience of ketogenic diet as an adjuvant therapy in Febrile Infection Related Epilepsy Syndrome (FIRES) | |
Purnima Suhas Prabhu, Vrajesh Udani, Toral Bhatt, Neelu Desai |
Ketogenic Diet (KD) in children with epilepsy: Parental expectations and experiences | |
Rajesh RamachandranNair, Nandini Nandeesha |
The role of sleep and awake EEGs in detection of epileptiform discharges in pediatric population. | |
Nupur Sinha, Shilpa Kulkarni, Suresh Birajdar, Tushar Maniar |
ketogenic diet in infant with intractable epilepsy | |
alifiani hikmah putranti |
Evolution and Outcome of Epilepsy in Children with Neonatal Hypoglycemic Brain Injury | |
Neeta Ajit Naik |
Clinical utility of next generation sequencing in Early-Onset Epileptic Encephalopathies | |
Vishal Sondhi, K M Adhikari, Vishal Vishnu Tewari, K Venkatnarayan, Rakesh Gupta |
Genotype and phenotype of epileptic patients with SCN2A mutations | |
Qi Zeng, Xiaoling Yang, Dan Wang, Jing Zhang, Jiaoyang Chen, Aijie Liu, Xiaoyan Liu, Xiru Wu, Yuwu Jiang, Yuehua Zhang |
Infantile epilepsy with multifocal myoclonus caused by TBC1D24 mutations | |
Jing Zhang, Jiaoyang Chen, Qi Zeng, Liping Zhang, Xiaojuan Tian, Xiaoling Yang, Zhixian Yang, Ye Wu, Yuehua Zhang |
Hypothyroidism and valproate: Is there a causal relationship? | |
Chhitiz Anand |
Epilepsy Versus Chronic diseases: How different are parent’s attitudes? | |
Noha El tantawi, Dina Abd Elmegid, Eman Atef |
The electroclinical features of CHD2 mutation related epilepsy | |
Jiaoyang Chen, Jing Zhang, Qi Zeng, Liping Zhang, Hua Li, Zhixian Yang, Xiaoling Yang, Aijie Liu, Yuehua Zhang |
Electrophysiological characteristics in children with Subacute sclerosing panencephalitis (SSPE): A study from a tertiary care hospital. | |
ANSHITA ARORA, SHILPA KULKARNI, MEENAL GARG, SONAM KOTHARI, ANAITA HEGDE, KRISHANKUMAR SHAH |
CLINICOETIOLOGICAL PROFILE OF CHILDHOOD SEIZURES IN A TERTIARY CARE HOSPITAL: A PROSPECTIVE OBSERVATIONAL STUDY | |
Akash Rai, Dipankar Gupta, Sankar Kumar Das |
Up-regulation of HMGB1-TLR4 Inflammatory Pathway in Focal Cortical Dysplasia Type II | |
Ye Wu |
Super Refractory Status Epilepticus in children : Etiological, electrophysiological, treatment and outcome profile | |
Deepti Ashok Kewalramani, Sonam Kothari, Shilpa Kulkarni, Anaita Hegde, Krishankumar Shah |
Does Ethnicity Affect the Clinical Presentation of Tuberous Sclerosis Complex? | |
Ravi Benjamin Dhamija, Cigdem Akman, Aliza Alter, Daniel McBrian, Elena Gonzalez |
Serum levels of both prolidase activity and oxidative stress in epileptic children | |
Nurettin KARACAN, Mustafa CALIK |
Role of Arterial Spin Labeling (ASL) in Localization of Epileptogenic Focus for Pre-surgical Evaluation of Intractable Epilepsy. | |
Rahul M Nikam, Vinay Kandula, Arabinda Choudhary, Harry Chugani |
Functional Hemispherotomy : patient characteristics and outcome in a series of 26 patients | |
Lakshminarayanan Kannan, Dinesh Nayak, Ravi Mohan Rao |
Clinical characteristics and epilepsy outcomes after surgery in children with focal cortical dysplasia type II | |
tianshuang wang, Ming Liu, Jie Zhang, Lixin Cai, Qingzhu Liu, Yuwu Jiang, Ye Wu |
Semiological, Diagnostic and theraupetic challenges in Infantile onset epilepsy | |
Smilu mohanlal, Lokesh lingappa, Ramesh Konanki, Nikit Shah, Srikanth Domala, Prasanthi Aripirala, Ravi verma |
KNOWLEDGE ATTITUDE PRACTICE (KAP) STUDY FOR THE CARE OF CHILDREN WITH EPILEPSY IN SCHOOLS | |
Darshana N Vora, Nitish S Vora |
Hemispherotomy for catastrophic epilepsy: our early experience | |
Sujit Abajirao Jagtap, Nilesh Kurwale, SANDEEP PATIL, SONAL CHITNIS, ANIRUDHA JOSHI, SUJIT NILEGAONKAR |
Vagal Nerve Stimulation treatment in children with pharmaco-resistant epilepsy: A single centre experience | |
Mazen Haider, Helen McCullagh, Gayatri Vadlamani, Janet Kellett, Gopalakrishnan Venkatachalam |
Clinical profile of patients with infantile spasms following Neonatal hypoglycemic brain injury: a retrospective study from India | |
Romit Jain, Prabhar Srivastava, Priyanka Surana, Vivek Jain |
Yield of Laboratory Testing in Pediatric Ketogenic Diet Patients: Critical Assessment of Abnormal Results and Impact on Clinical Care. | |
Charuta Joshi, Chelsey Stillman, Stephanie Criteser, Alison Conley, Jennifer Oliver |
Simultaneous quantification of alpha-aminoadipic semialdehyde, piperideine-6-carboxylate, pipecolic acid and alpha-aminoadipic acid in pyridoxine-dependent epilepsy | |
Zhixian Yang, Jiao Xue, Pan Gong, Junjuan Wang, Minhang Wu, Wenshuang Yang, Shiju Jiang, Ye Wu, Yuwu Jiang, Yuehua Zhang, Tatiana Yuzyuk, Hong Li |
COMPARISON OF CALCIUM LEVELS IN CHILDREN WITH FEBRILE SEIZURES AND CHILDREN WITH FEVER AND NO SEIZURES | |
Rekha Mittal, Shailabh Gupta, Naresh Bhatia |
Some Neuropsychological factors as associated to cognitive functions of Mesial Temporal lobe epilepsy (MTLE) children. | |
Gopukumar Kumarpillai, Murthy G, Umashankar R, shobha Nandavar, Girish Gadre |
Nitrazepam as first line treatment for Infantile Spasm-20 years’ experience from Tertiary Paediatric Neurosciences Centre | |
Jay Shetty, Paul Eunson, Celia Brand, kenneth McWilliam, Krishnaraya Kamath Tallur, Richard Chin, Ailsa McLellan |
Low ratio ketogenic diet (KD) can achieve good seizure control in children with epilepsy | |
Rajesh RamachandranNair, Zeling Chen |
Outcome Following Febrile Seizures: A Scottish Population Cohort | |
Libby CHATTERTON DICKSON, Ailsa McLellan, Paul Leonard, Clodagh Mitchell, Jay Shetty |
PHOTOSENSITIVITY AND CLINICAL CHARACTERISTICS FROM A SCOTTISH POPULATION COHORT | |
Gareth Neo, Lauren Marie Smith, Leanne Brennan, Jay Shetty, Krishnaraya Kamath Tallur |
Experience with Isoflurane in Paediatric Super Refractory Status Epilepticus | |
Ashwini Mohan, Lokesh Lingappa, Ramesh Konanki, Nikit Shah, Smilu Mohanlal, Farhan Shaikh, anupama Y, shashwat Mohanty |
Effects rehabilitation with interactive metronome training on speech disorders and epilepsy patients. | |
Tatiana Tomenko |
Epilepsia Partialis Continua (EPC) in children: Clinical presentation and underlying aetiologies | |
SNEHAL SURANA, Jane Hassell, Stewart Boyd, Helen Cross, Yael Hacohen |
An Exploration of Prescribing Practice and Parental Use of Emergency Rescue Medication to Prevent Status Epilepticus in Children | |
Celia Brand, Ailsa McLellan |
Protective effects of the ROCK inhibitor fasudil against cognitive dysfunction following status epilepticus in immature male rats | |
Song xiaojie |
Our experience with use of new 2017 ILAE classification in children with epilepsy | |
Abhinav Sahu, Neeta Naik, AMI SHAH, Abhinav Tiwari |
A Study of Reasons for Poor Response/ Poor Control of Epilepsy in Children on Polytherapy | |
nilima narkhede |
MAGNITUDE OF CO-MORBIDITIES IN PEDIATRIC EPILEPSY: NEED FOR NEUROPSYCHOLOGICAL REHABILITATION | |
Somini Haresh Mehta, Urvashi Shah |
Epilepsy burden in NHBI (Neonatal Hypoglycemic Brain Injury) | |
RITESH C SHAH |
Retrospective cohort of Dravet syndrome due to SCN gene mutation from Southern India | |
Hemadriben Muljibhai Vegda, Vykuntaraju Gowda, Raghavendraswami Amoghimath, Asha benakappa |
Evolution of electroencephalogram findings in pontocerebellar hypoplasia type 2A | |
Rony Cohen, Yoram Nevo, Sara Kivity, Ayelet Halevy, Sharon Aharoni, Rachel Straussberg |
Infantile tremor syndrome followed by West Syndrome: A case series | |
Jasmine Singh |
Tolerance to cannabidiol in children and adults with treatment-resistant epilepsy | |
Shimrit Uliel-Sibony, Moran Hausman-Kedem, Uri Kramer |
EPILEPTIC ENCEPHALOPATHY DUE TO GABRG2 MUTATION | |
Angeles Schteinschnaider, Isaura Gonzalez, Eliana Julian, Julia Boccoli |
Efficacy of zinc supplementation in preventing recurrence of febrile seizure in Bangalore | |
Ramya Ramesh, Rachel Ranitha Peterson, Carolin Elizabeth George |
Two novel PCDH19 missense mutations in a mosaic male and a female epilepsy patients | |
Qian Peng, Haiming Yuan |
systematic review of Perampanel in children and adolescent | |
ALPANA SANTOSH KONDEKAR, Rochana Redkar |
Verbal Semantics and Social cognition in adolescents with drug resistant refractory epilepsy | |
Sujit Abajirao Jagtap, SONAL CHITNIS, KINJAL JAIN, ANKIT ARORA, MEDHA ADHYRU, SANDEEP PATIL, NILESH KURWALE |
A hot and jerky child | |
Sonal Bhatia |
Comparison of 1981, 1989 and 2017 International League Against Epilepsy classification (ILAE) | |
David Asish Manchala, Neelu Desai, Payal Shah, Vrajesh Udani |
Assessment of quality of life in Omani children with epilepsy attending Sulatan Qaboos University Hospital | |
Amna Mohamed Al Futaisi |
Mammalian Target of Rapamycin (mTOR) Inhibitors as an Effective Therapy for Refractory Epilepsy associated with Tuberous Sclerosis Complex: A Systematic Review | |
ALPANA SANTOSH KONDEKAR, mayank Detroja |
Dandy Walker malformation with epileptic spasms | |
Gürkan Gürbüz |
Effectiveness and Safety of high-dose, Oral Pyridoxine as an adjunct to high-dose Adrenocorticotrophic hormone versus high-dose Adrenocorticotrophic hormone alone for the treatment of West Syndrome: An Open-Label, Randomized Control Trial | |
Arundhati Banerjee, Jitendra Kumar Sahu, Naveen Sankhyan, Smita Pattanaik, Renu Suthar, Arushi Gahlot Saini, Lokesh Saini, Prahbhjot Malhi, Pratibha Singhi |
SPECTRUM OF TUBEROUS SCLEROSIS COMPLEX - CLINICAL PROFILE IN A COHORT OF 48 CHILDREN | |
Leema Pauline Cornelius |
Valproic Acid: A potion with caution | |
ALPANA SANTOSH KONDEKAR, swarupa bansode |
Etiology of Epilepsy In a developing Country – A study from a tertiary Pediatric Hospital | |
David Asish Manchala, Neelu Desai, Rahul Badheka, Vrajesh Udani |
Bones and brains: a prospective case-control study of seasonal vitamin D in childhood epilepsy | |
Celia Brand, Ailsa McLellan, Sonia Joseph, Richard Chin |
X-LINKED EPILEPTIC INFANTILE ENCEPHALOPATHY OF UNUSUAL INHERITANCE | |
Angeles Schteinschnaider, Solange Gril, Mercedes Villanueva, Agatha Fernandez, Horacio Martinetto, Ezequiel Surace |
SYNCOPE IN CHILDREN-CLINICO-ETIOLOGICAL CORRELATION | |
MADHURA FADNIS |
Severe neonatal epileptic encephalopathy secondary to a mutation of the ATP1A3 gene | |
Thouraya Ben Younes, Hanene Benrhouma, Hedia Klaa, Aida Rouissi, Myriam Chaabouni, Ichraf Kraoua, Ilhem Ben Youssef-Turki |
Telephone based follow-up of children with Epilepsy aged 4 months to 18yrs: comparison of accuracy between a Specialty Nurse and a DM Pediatric Neurology Fellow to identify Critical Clinical Events requiring Face-to -Face evaluation | |
Sheffali Gulati, Prashant Jauhari, Shruti N M, Prateek Kumar Panda, Mable Jossy, Biswaroop Chakrabarty, R M Pandey |
Epilepsy in Children- Psychosocial and Emotional Impact on Their Siblings and Their Coping Skills | |
EKTA AGARWAL, Dr. Kavita Srivastav, Dr. Surekha Rajadhyaksha, Dr. Manjiri Datar |
LANGUAGE EVALUATION IN GENETIC EPILEPSY FEBRILE SEIZURES + SYNDROME – A PROSPECTIVE CONTROLLED OBSERVATIONAL STUDY | |
Toral Bhatt, Vrajesh Udani, Megha Shah, Neelu Desai, somini mehta |
EFFECT OF LONG-TERM ANTIEPILEPTIC DRUGS ON BONE MINERAL METABOLISM AND THYROID PROFILE IN INDIAN CHILDREN:A CASE CONTROL STUDY | |
Devaraja Sethi, Kavita Srivastava, Surekha Rajadhyaksha, Anuradha Khadilkar |
Epidemiological Survey (three staged) of Pediatric Epilepsy in a rural suburb of Pune District | |
EKTA AGARWAL, Dr. Surekha Rajadhyaksha, Dr. Kavita Srivastav |
Clinical and therapeutic profile of childhood epilepsy in an Onchocerciasis-endemic rural Area | |
Dominique ENYAMA |
Asymptomatic malaria parasitaemia and seizure control in children with nodding syndrome; a cross sectional study | |
Rodney Ogwang, Ronald Anguzu, Pamela Akun, Albert Ningwa, Edward Kayongo, Kevin Marsh, Charles Newton, Richard Idro |
Prevalence of Seizures among children admitted with BRUE (Brief resolved unexplained event) | |
Lamyaa Jad |
EFFECT OF ACTH COMBINATION THERAPY VERSUS ACTH ALONE IN WEST SYNDROME: A RETROSPECTIVE STUDY | |
Devaraja Sethi, Kavita Srivastava, Surekha Rajadhyaksha |
Clinical Profile of Epilepsy in Neonatal Hypoglycemic Brain Injury. | |
Madhavi Shelke, Shirish Bhartiya, Varsha Vaidya, Sandeep Saraf |
Kabuki Syndrome and Effectiveness of Perampanel | |
Manoj Vasireddy |
Comparison between Melatonin and Diazepam for Prevention of Recurrent Simple Febrile Seizures: Randomized clinical trial | |
amira darwish |
Clinical spectrum and therapeutic outcomes of electrical status epilepticus during sleep in children | |
Bing-Wei PENG, Hai-Xia Zhu, Xiu-Ying WANG, Xiao-Jing LI, Hui-Ci LIANG, Feng-Qiong ZHANG, SHu-Yao Ning, Yan-Ying Zhong, Wen-Xiong Chen |
Febrile Infection Related Epilepsy Syndrome (FIRES) – A rare cause of super refractory status epilepticus | |
Aanchal Pradeep Khemani, Sanjay Bafna, Sagar Lad, Nandan Yardi |
Clinicoetiological profile and outcome of convulsive status epilepticus in children | |
Rajwanti Kishore Vaswani, Sayoni RoyChowdhury |
“Me and My Epilepsy”: A qualitative study of Children’s Experiences and a novel child-centered animation about epilepsy | |
Rebecca Black, Jeni Harden, Martyn Pickersgill, Jay Shetty, Ailsa McLellan, Celia Brand, Michelle Small, Richard Chin |
Neonatal-onset epilepsy: Clinico-etiological spectrum and short-term outcome | |
Prasanthi Aripirala, Ramesh Konanki, Lokesh Lingappa |
Utility of short term video EEG recording in diagnosis of paroxysmal events in children | |
abhinav ashok tiwari, neeta naik, ami shah, abhinav sahu |
Polypharmacy in childhood epilepsy syndrome management: overuse or underuse of a diagnostic tool? | |
selina husna BANU, SELINA HUSNA BANU, Naila Zaman KHAN |
Continuous Spikes and Waves during Slow-Wave Sleep (CSWS) in Children: The Epilepsy Syndrome that Can’t Stop, Won’t Stop | |
Arushi Gahlot Saini, Naveen Sankhyan, Prahbhjot Malhi, Niranjan Khandelwal, Pratibha Singhi |
Infantile spasms following Acquired brain injury - A tertiary Neuro-Rehabilitation centre experience | |
Archana Murugan |
Oral Ketamine is an Effective and Safe Treatment for Non-Convulsive Status Epilepticus | |
Archana Murugan |
A Prospective Study of Non-Epileptic Events in Children with Intractable Epilepsy | |
Shermila Pia, Andrew Mallick, Elliot Warren, Nick Kane |
Transition to adult medical care for adolescents with epilepsy-identifying care gaps in current models: Perspectives from a UK neurology tertiary centre | |
Thomas Robb |
EPEMA (encephalopathy,petechiae and ethylmalonic aciduria) – a case series. | |
KAPIL JETHA, Vykuntaraju K Gowda, Varun M Srinivas, Meenakshi Bhat, Maya Bhat, Christopher Rita, Asha Benkappa |
Cohort of Clinical profile and Outcome of Pyridoxine dependent epilepsy | |
KAPIL JETHA, Vykuntaraju K Gowda |
Headache
Barriers to Care among Indian Children with Recurrent Headache | |
Charu Jain, Devendra Mishra, Monica Juneja, V Pavithra, Deepti Chawla |
The Perception and Performance of Headache Management among School Health Teachers | |
Young-Il Rho, Shin-Young Park, Mi-Sun Jang |
Examination of children with migraine; Three years experience | |
Deniz Karakaya, Deniz Yüksel, Hülya Kayılıoglu, Ayşe Aksoy, Ulkuhan Oztoprak, Çigdem Genç Sel, Erhan Aksoy, Ozge Dedeoglu |
COMPARISON OF THE LIFESTYLE PATTERNS OF CHILDREN WITH RECURRENT PRIMARY HEADACHE WITH THOSE OF CHILDREN WITH NO HEADACHE IN FIVE TO EIGHTEEN YEARS AGE | |
Rekha Mittal, Lakshmi Narain Taneja, Sumit Kumar Dwivedi |
Factors Predicting Migraine in Pediatrics Patients with Asthma: A National Perspective | |
Riddhiben patel, vandana vedanarayanan, jagdish desai |
P300 scores and neurobehavioural profile of children with primary headache | |
Jyotindra Narayan Goswami, Saroj Kumar Patnaik |
Relapsing factors for pediatric migraine | |
KON-HEE LEE |
Arterial Spin Labelling Perfusion Weighted Imaging (ASL-PWI) in Pediatric Hemiplegic Migraine: Clinico-radiological Correlation | |
Badal G Jain, Rahul Nikam, Tara Pezzuto, Rachit Patil, Vinay Kandula |
Assessment of the association between pediatric Idiopathic Intracranial Hypertension and olfactory function | |
Maya Muhlbauer Avni, Naama Yosha-Orpaz, Osnat Konen, Nitza Goldenberg-Cohen, Rachel Straussberg |
IDIOPATHIC INTRACRANIAL HYPERTENSION IN CHILDREN- IS IT REALLY IDIOPATHIC? | |
Sumeet Rajendra Dhawan, Lokesh Saini, Raviteja Indla, Indar Sharawat, Akshay Saxena, Sameer Vyas, R K Sharma, Arushi Gahlot Saini, Renu Suthar, Jitendra Sahu, Naveen Sankhyan |
Metabolic Disorders
Pyridoxine dependent epilepsy: beyond ALDH7A1 gene mutation | |
ROSHAN KOUL |
A RARE CAUSE OF STRIDOR & RECURRENT CENTRAL APNEA: MAPLE SYRUP URINE DISEASE | |
RAVI SHARMA, SAKSHI SHARMA, VIVEK JAIN, LALIT BHARADIA |
DIAGNOSIS OF GM2 GANGLIOSIDOSIS WITH A NEW MUTATION | |
Rashmi Adiga, Neha Rajkumar Jain, Sudhindra Kulkarni, Kruti Varshney |
Leigh-like syndrome due to homoplasmic m.8993T>G variant with hypocitrullinemia and unusual biochemical features suggestive of multiple carboxylase deficiency (MCD) | |
Maina Padmanabha Kava, Barry Lewis, Lawrence Greed, Shanti Balasubramaniam |
Large-single scale mitochondrial DNA deletions in different tissues of patients with Kearns-Sayre syndrome | |
yuqing shi, fang fang, zhimei liu |
Long-term follow-up and Clinical findings of BH4 deficiency patients in Korea | |
Eun Sook Suh |
Three Cases Of Creatine Deficiency Syndromes Caused By GAMT Gene Mutation | |
Lei Yang, Fang Fang |
Expanding the phenotype of TRNT1 mutations to include Leigh syndrome. | |
Carolina Gorodetsky, Chantal F. Morel, Ingrid Tein |
Fatal neonatal lactic acidosis secondary to a novel defect in COX16 causing complex IV deficiency | |
Maina Padmanabha Kava, Shanti Balasubramaniam, Barry Lewis, Richard Rodenburg |
TRPM6 gene mutation resulted in primary hypomagnesemia with secondary hypocalcemia(HSH) in 3 cases | |
xiaohui wang, shen zhang, weihua zhang, jiuwei li, changhong ding, fang fang |
NEWLY IDENTIFIED TOTALLY TREATABLE METABOLIC ENCEPHALOPHY: Biotin-Thiamine Responsive Basal Ganglia Disease | |
TARISHI NEMANI, PUJA MEHTA, Purva Keni karnavat, ANAITA UDWADIA HEGDE |
Phosphoserine aminotransferase deficiency: MRI Findings. | |
Alcy Torres, Zakir Iqbalbhai Shaikh, Bindu Setty |
Biotin-Thiamine-Responsive Basal Ganglia Disease: A Case Presentation | |
Ceren Günbey, İnci Türkan Yılmaz, İbrahim Taş, Meral Topçu |
Profile of Peroxisomal Disorders in infancy and childhood | |
Lobna Abdelgawad Mansour, Ekram Mohamed Fateen, Mohamed Ahmed Rashed, Hoda Ahmed Marzouk, Dina Mohamed Hesham, Lamia Tarek Tawfik |
Argininemia in 3 siblings- different phenotypes in the same family | |
Aman Elwadhi, Suvasini Sharma, Bijoy Patra |
Gene therapy improves global development in AADC deficiency | |
Takanori Yamagata, Karin Kojima, Akihiko Miyauchi, Takeshi Nakajima, Naoyuki Taga, Sachie Nakamura, Mitsuhiro Kato, Hitoshi Osaka, Shin-ichi Muramatsu |
Hypocalcemia as a cause of breath holding spells in children below 6 months | |
Simran Jain, Neha Ahuja, Gouri Rao Passi |
An unusual presentation of Menkes disease masquerading as a leukodystrophy with macrocephaly | |
Aswini Annadurai, Anshula Tayal, Aman Elwadhi, Suvasini Sharma, Bijoy Patra |
A rare cause of developmental delay | |
Sakshi Batra, Aman Elwadhi, Suvasini Sharma, Bijoy Patra |
A case report on siblings with motor regression and dystonia | |
Abhishek Jain, Aman Elwadhi, Suvasini Sharma, Bijoy Patra |
Neurometabolic profile of macrocephaly in infancy and childhood, Biochemical and molecular study | |
Lobna Abdelgawad Mansour, Ekram Mohamed Fateen, Mohamed Ahmed Rashed, Ezzat Mohamed Elsobky, Solaf Mohamed Mohamed, Lamia Tarek Tawfik |
Case of two brothers with Cerebrotendinous Xanthomatosis presenting with Progressive Myoclonic Epilepsy | |
Karan Desai, Sangeeta Ravat, Viraj Sanghi, Piyush Kumar, Priyanka Walzade, Neeraj Jain |
A case series of four patients of Menkes disease -clinico radiological presentation with usual and unusual features. | |
umesh dinkar kalane, Umesh Dinkar Kalane, Surekha Rajadhyaksha |
Assessment of Vitamin B-12 deficiency and Risk Factors in Healthy Infants: A Cross-sectional Study | |
Kuchana Suresh Kumar, Savita Attri, Arushi Gahlot Saini, Bhavneet Bharti, Naveen Sankhyan, Prateek Bhatia, Ajay Patial |
Gelastic cataplexy leading to the diagnosis of Niemann-Pick disease type C | |
Ezgi Oktener Anuk |
CONGENTIAL METHEMOGLOBINEMIA TYPE 2: A RARE CAUSE OF NEURODEVLOPMENTAL DELAY | |
vishal bhansali, sanjay bafna |
BIOTINIDASE DEFICIENCY: A TREATABLE CAUSE OF REFRACTORY EPILEPSY IN INFANCY | |
SHIKHA JAIN |
Clinical and genetic analysis in three Chinese patients with congenital disorder of glycosylation | |
Changhong Ren, Fang Fang, Changhong Ding |
GLUTARIC ACIDURIA TYPE 1: AN USUAL IMAGING FEATURE | |
SHRUTI HARSHAL AGRAWAL, SANGEETA RAVAT, VIRAJ SANGHI |
Spectrum of Inherited White Matter Disorders in Children and their Outcomes | |
Vijay Gonda, Arushi Gahlot Saini, Naveen Sankhyan, Jitendra Sahu, sameer vyas, Savita Attri, Inusha panigrahi |
Kangaroo gait as a presentation of Hyper-manganesemia | |
Akash Harakchand Chheda, Vrajesh Udani, Hina Faldu |
All that glitters is not gold: A lesson to learn. | |
abhijeet vilas botre |
Lysine- restricted diet in a child with pyridoxine -dependant epilepsy prevents long term developmental delay | |
Leah Queit, Maina Padmanabha Kava, Barry Lewis, Lawrence Greed, Peter Williams Rowe, Shanti Balasubramaniam |
Treatable Leigh syndrome involving mitochondrial cofactor metabolism | |
Zhimei Liu, Fang Fang |
Infantile-onset mitochondrial disorder associated with COQ4 missense mutations | |
Leechin Wong, WangTso Lee |
Does Thiamine help in Wilsons disease management? | |
MAHESH ARUN SAMBHARE |
Pediatric neurotransmitter disorders: single center experience in India | |
Rahul Badheka, Vrajesh Udani, Neha Inamdar |
Clinico-biochemical profile and outcome of children with Inborn Errors of Metabolism (IEM) | |
Bidisha Banerjee, Supriya Shinde, Rita Christopher |
A novel mutaion in HTRA2 causes mitochondrial disorder associated with early infantile onset epileptic encephalopthy,movement disorder and 3 methyl glutaconic aciduria | |
Harshkumar Arvindbhai Patel |
A proposed staging system for CLN3 disease (Juvenile Batten Disease) | |
Jonathan W Mink, Justin Williams, Erika Augustine |
MTHFR Deficiency Heavy Form going with Demyelinating Leukodystrophy and Psychomotor Retardation | |
MESUT GUNGOR, BULENT KARA |
The Clinical feature of Urea cycle disorders in China | |
Li Jiang |
Analysis of 154 cases with mitochondrial DNA variations in Chinese children with mitochondrial disorders | |
yuqing shi |
The Unified Batten Disease Rating Scale (UBDRS): Validation and Reliability in an Independent Sample | |
Jonathan W Mink, Miriam Nickel, Eva Wibbeler, Christoff Schwering, Angela Schulz |
Resting state cerebral glucose metabolism using [18]Fluoro-Deoxy-Glucose-Positron Emission Tomography (FDG-PET) imaging and motor and sensory neurophysiology in children with Glutaric Aciduria(GA1) dystonia awaiting Deep Brain Stimulation Surgery (DBS) | |
Stavros Tsagkaris, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Keyoumars Ashkan, Richard Selway, Verity McClelland, Alexander Hammers, Jean-Pierre Lin |
Clinical and genetic analysis of progressive cavitating leukoencephalopathy in China | |
Ren Changhong, Fang Fang, Zhimei Liu |
NEUROREGRESSION IN CHILDREN – CLINICAL SPECTRUM AND INVESTIGATION PROFILE IN CHILDREN ATTENDING NEUROLOGY OUTPATIENT | |
Ayesha Mariam, vishwanathan venkataraman |
Clinical profile of Indian children with type 1 citrullinemia at a Tertiary care referral centre in Southern India – A Descriptive study | |
Balamurugan N, Vykuntaraju K Gowda, Rita Christopher, Asha Benakappa |
Clinical profile of children with type 1 Glutaric aciduria at a Tertiary care referral centre in Southern India – A Descriptive study | |
Balamurugan N, Vykuntaraju K Gowda, Varunvenkat M Srinivasan, Asha Benakappa |
Spectrum of riboflavinopathies from southern India - A desrciptive study | |
Arundhati Patil |
Severe preeclampsia could be the sign of long-chain fatty acid oxidative enzyme deficiency | |
Selda Bülbül, Uğur Can Kara |
Lysosomal Storage Diseases: Experiences of Kırıkkale University | |
Selda Bülbül, Cansu Çelik, Elif Gökçe Ünal |
Importance of Influenza vaccination in Urea Cycle Disorders | |
Selda Bülbül, Cansu Çelik, Elif Gökçe Ünal |
Movement Disorders
A novel frameshift mutation in SLC2A1 (GLUT1) associated with a mild form of carbohydrate-responsive movement disorder | |
Yasser Awaad |
High dose of levodopa and Segawa disease | |
Madina Taghiyeva |
GENETIC SPECTRUM OF PEDIATRIC MOVEMENT DISORDERS | |
Kritika Tiwari, TARISHI NEMANI, Purva Keni karnavat, ANAITA UDWADIA HEGDE |
Utility of Deep Brain Stimulation in Pantothenate Kinase Associated Neurodegeneration(PKAN) | |
Puja Mehta, Purva Keni, Anaita Hegde |
Management of Status Dystonicus in Children: Reporting of 3 cases with videos. | |
Kanij Fatema |
A Rare Case Of Early Onset Hereditary spastic paraplegia caused by AFG3L2 and SPG7 mutations | |
Piyush Kumar Anshu, Dr Viraj Sanghi |
Paroxysmal exercise induced dyskinesia in siblings — A rare cause | |
Senthilkumar Vajramanickam |
An Imaging Clue for Treatable Early Childhood-Onset Dystonia - Manganism | |
Hansashree Padmanabha, Savita Krishnamurthy, Sharath Kumar G G, Indumathi Chikkanayakana |
Anti-NMDAR Encephalitis in Children ; a Malaysian Experience | |
Balakrishnan Priyalatha, Tajudin Tajul Arifin, Vigneswari G |
Rett syndrome in Taiwan: genotype and phenotype characteristics | |
Leechin Wong, WangTso Lee |
Atypical Presentations of Anti-NMDAR encephalitis – A Report of 3 Interesting Cases | |
Balakrishnan Priyalatha, Tajudin Tajul Arifin |
Two Different Phenotypes of Tyrosine Hydroxylase Deficiency Syndrome | |
Punita Chandra Segaran, Tajudin Tajul Ariffin |
A tripping kid- Unusual presentation of GLUT 1 Deficiency Syndrome | |
Jigyasha Sinha, Anirban Ghosal, Hrishikesh Kumar |
Transcranial magnetic stimulation in the treatment of Tourette's syndrome in children: A pilot study | |
Cynthia K Kahl, Adam Kirton, Tamara Pringsheim, Paul Croarkin, Rose Swansburg, Ephrem Zewdie, Frank P MacMaster |
Spectrum of movement disorders in children – types, etiology, severity and response to therapy | |
Chandrashekhar Pandey, Hardeep Singh Malhotra, Chandrakanta Kumar, Rashmi Kumar |
Unusual Presentation of 4H Syndrome as Post Varicella Ataxia | |
Ridhimaa Jain, Aman Elwadhi, Suvasini Sharma, Nicole Wolf, Resie M van Spaendonk, Bijoy Patra |
PROGRESSIVE AND SEVERE MOVEMENT DISORDER IN A PATIENT CARRYING A GNAO1 MUTATION RESPONSIVE TO DEEP BRAIN STIMULATION | |
Angeles Schteinschnaider, Mercedes Villanueva, Milagros Beltramo, Agata Fernandez, Ezequiel Surace, Horacio Martinetto |
THE EFFECT OF RISPERIDONE IN IMPROVING MOTOR AND FUNCTIONAL DISABILITY IN CHILDREN WITH CHOREO-ATHETOID CEREBRAL PALSY: A ONE YEAR PROSPECTIVE STUDY AT A TERTIARY CARE CENTRE | |
Nishant Mittal |
“Distinctive upper limb dystonia as a correlate to the ‘Eye of tiger’ MRI sign.” | |
Akash Harakchand Chheda, Satish Khadilkar, Vrajesh Udani |
CHILDHOOD ONSET CHRONIC ATAXIA: A CLINICAL, ETIOPATHOLOGICAL, RADIOLOGIC AND GENETIC AUDIT. | |
Pallavi Shriram Todase, shilpa kulkarni, sonam kothari, anaita hegde, krishankumar shah |
Can early onset ataxia phenotypically be distinguished from developmental coordination disorders? | |
Tinka Lawerman, Rick Brandsma, Natasha M Maurits, Octavio E Martinez-Manzanera, Roelineke J Lunsing, Oebele F Brouwer, Hubertus PH Kremer, Deborah A Sival |
A novel mutation in KMT2B gene causing childhood-onset generalized dystonia | |
Tanmayee Subhash Thombare |
A Diagnostic Algorithm for Early Onset Ataxia | |
Rick Brandsma, Corien Verschuuren, Oebo Brouwer, Hubertus Kremer, Tom de Koning, Marina de koning-Tijssen, Deborah Sival |
Clinical clues in etiological diagnosis of childhood ataxia | |
EKTA AGARWAL |
Profile of Neuronal Brain Iron Accumulation in Pediatric population: experience from a tertiary care centre in North India | |
Ankita Pal, Prateek Kumar Panda, Biswaroop Chakrabarty, Prashant Jauhari, Vishal Sondhi, Rajni Farmania, Atin Kumar, Manisha Jana, Sheffali Gulati |
Early Onset Ataxia and Comorbid Dystonia: Are There Shared Biological Pathways? | |
Deborah Anita Sival, Marina Tijssen, Dineke Verbeek |
PONTOCERREBELAR HYPOPLASIA SUBTYPE 1B (EXOSC3 MUTATION): CASE REPORT | |
Fernanda Noemi Moreira, Nicolas Espinosa |
Tics in a child with Hashimoto encephalopathy | |
Padma Balaji, Vasanthi Thiruvengadam, Ashish Badaya |
Writer’s cramp in children- A case series | |
dipa saha |
Multimodal immunotherapy in a patient with opsoclonus-myoclonus-ataxia syndrome - case report | |
Tomasz Mieszczanek |
The Tonic Labyrinthine Response (TLR) also known as “Scissoring” is a hallmark of Dystonia | |
Federica Graziola |
Spinocerebellar ataxia 35 | |
Manimala S |
Status dystonicus in Children: A Nightmare for both the Physician and the Patient | |
Arushi Gahlot Saini, Kanika Goyal, Sumeet Dhawan, Lokesh Saini, Renu Suthar, Jitendra Sahu, Naveen Sakhyan, Jayashree Muralidharan, Pratibha Singhi |
Motor and sensory neurophysiology in childhood dystonias correlate with distinct resting glucose brain metabolism patterns using [18F]FDG PET-CT imaging and may help characterise the prognosis of deep brain stimulation (DBS) neuromodulation | |
Stavros Tsagkaris, Verity McClelland, Sinead Barkey, Maiju Kattelus, Lesley Baker, Sarah Perides, Daniel Lumsden, Margaret Kaminska, Hortensia Gimeno, Teresa Szyszko, Alexander Hammers, Jean-Pierre Lin |
Tourette syndrome -a developmental dopamine disorder | |
Yoshiko Nomura |
Segawa Disease- 47 years since the first description -Revisit of its clinical features and pathophysiology | |
Yoshiko Nomura |
Muscle and Nerve
Incidence of infantile spinal muscular atrophy in Shikoku Island of Japan | |
Kentaro Okamoto, Mitsumasa Fukuda, Isao Saito, Risako Urate, Satoshi Maniwa, Daisuke Usui, Takahiro Motoki, Toshihiro Jogamoto, Kaori Aibara, Takatoshi Hosokawa, Yukihiko Konishi, Reiko Arakawa, Kenji Mori, Eiichi Ishii, Kayoko Saito, Hisahide Nishio |
Rigid spine syndrome: A report of 15 children | |
ROSHAN KOUL |
Childhood Onset Limb Girdle Muscular Dystrophies in Aegean Part of Turkey | |
Uluç Yiş, Gülden Diniz, Filiz Hazan, hülya sevcan daimagüler, bahar toklu baysal, figen baydan, gülçin akıncı, aycan ünalp, gül aktan, erhan bayram, semra hız, cem paketçi, derya okur, erdener özer, ayça ersen danyeli, gökhan uyanık, sebahattin çırak |
Differentiation between inflammatory myopathies and genetic muscle disease | |
xingzhi chang |
Diagnostic Potential of Next Generation Sequencing in Suspected Genetic Neuromuscular Disorders | |
Dr Vishal Kanubhai Patel, Purva Keni Karnavat, Anaita Udwadia Hegde |
Spinal Muscular Atrophy – Lower Extremity Dominant Type 2 (SMALED2) | |
Erdem Simsek, Sanem Yilmaz, Hepsen Mine SERIN, Seda Kanmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben |
UK initiative to speed up diagnosis of Duchenne muscular dystrophy worldwide | |
Henriette van Ruiten, Mayhew Anna, Helen Aspey, Robert Muni Lofra, Volker Straub, Michela Guglieri |
Pain prevalence and characteristics in spinal muscular atrophy type II | |
Yuu Uchio, Mikiko Hasegawa, Kouta Kajima, Hayato Suzuki, Kaho Nakamura, Midori Saito, Tetsuo Ikai, Futoshi Wada, Kayoko Saito, Reiko Arakawa, Osamu Nitta |
Atypical childhood-onset neuroaxonal dystrophy in an Indian girl - case report | |
Himani Bhasin, Sakshi Jain, Marta Romani, Enza Maria Valente, Suvasini Sharma |
STUDY OF CYTOKINE (IL-2, IL-6, TNF-α, Interferon-ϒ, IL-17) LEVELS IN ACUTE GUILLAIN-BARRE SYNDROME | |
JAYANTH KRISHNA MADUGULA |
Neuromusclar transmission defect in FKRP congenital muscular dystrophy | |
Kenneth McWilliam, Linda McLellan, Lisa Robertson |
Bone Health Monitoring In Boys With Duchenne Muscular Dystrophy: A Survey Of Clinical Practice In The United Kingdom NorthStar Clinical Network | |
Shuko Joseph, Nadia Capaldi, Marina DiMarco, Iain A Horrocks, Volker Straub, S Faisal Ahmed, Michela Guglieri, Sze Choong Wong, North Star Clinical Network |
The Efficacy of Acyclovir in Childhood Bell’s Palsy | |
Gürkan Gürbüz |
Received care by brazilian patients with Duchenne Muscular Dystrophy | |
Clarisse Pereira Dias Drumond Fortes |
Combination of Topiramate and Lacosamide is Effective for Paramyotonia Congenita with neurological symptoms | |
Yoshie Kurokawa, Akihiko Miyauchi, Akihiko Miyauchi, Hirokazu Yamagishi, Hirokazu Yamagishi, Eriko Jimbo, Eriko Jimbo, Kazuhiro Muramatsu, Kazuhiro Muramatsu, Hitoshi Osaka, Hitoshi Osaka, Takanori Yamagata, Takanori Yamagata |
Impact of genetic results on treatment of CONGENITAL MYASTHENIC SYNDROME (CMS) | |
RINI KOTHARI, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, BINDU MADHAVI PARICHURI, SMILU MOHANLAL |
A Toddler with Myasthenia Gravis Ocular | |
alifiani hikmah putranti |
Vamorolone, the first dissociative steroidal anti-inflammatory, improves muscle function and shows limited side effects in Duchenne muscular dystrophy (DMD): results of Phase IIa studies in 48 DMD boys. | |
Michela Guglieri, Kanneboyina Nagaruja, Paula Clemens, Jesse Damsker, John McCall, Edward Smith, Diana Castro, Jean Mah, Craig McDonald, Nancy Kuntz, Richard Finkel, Mar Tulinius, Yoram Nevo, Monique Ryan, Richard Webster, Andrea Smith, Lauren Morgenroth, Eric Hoffman, Laurel Mengle-Gaw, Laurie Conklin |
CONGENITAL MYASTHENIA SYNDROME: CLINICAL PROFILE, TREATMENT RESPONSE, ELECTRODIAGNOSTIC STUDIES AND GENETIC AUDIT . | |
Pallavi Shriram Todase |
Guillain-Barre Syndrome: Uncommon association to common pediatric diseases | |
Marwa Abd Elmaksoud, Yasmine El Chazli, Shaymaa Elsayed |
Design of a phase 3 trial to evaluate the long-term efficacy and safety of ataluren in patients with nonsense mutation Duchenne muscular dystrophy | |
Francesco Bibbiani, Panayiota Trifillis, Edward O'Mara, Joseph McIntosh |
Long-term Pulmonary Function Outcomes in Non-Ambulatory Patients with Nonsense Mutation Duchenne Muscular Dystrophy Treated with Ataluren: 240-Week Data from an Open-label Extension Study | |
Craig M McDonald, Craig Campbell, Eugenio Mercuri, Francesco Muntoni, Kathryn Selby, Francesco Bibbiani, Panayiota Trifillis, Joseph McIntosh, Marcio Souza, Stuart W Peltz, Mar Tulinius |
CARDIOPULMONARY ASSESSMENT IN CHILDREN WITH DUCHENNE MUSCULAR DYSTROPHY | |
Priyanka Madhukar Meshram |
Late onset LAMA-2 Deficiency Congenital Muscular Dystrophy | |
Amarinder Singh Oberoi, Krishnakumar N Shah |
Ragged red fibers in myopathy with white matter changes - mitochondrial disorder or a red herring? | |
Bijoy Patra, Helman Guy, Suvasini Sharma, Puneet Jain, Ravinder Kumar Saran, MS Van Der Knapp |
Meta-analyses of ataluren in patients with nonsense mutation Duchenne muscular dystrophy | |
Craig Campbell, Francesco Muntoni, Eugenio Mercuri, Gary L Elfring, Panayiota Trifillis, Francesco Bibbiani, Stuart W Peltz, Craig M McDonald |
Preservation of Function over time as Measured by North Star Ambulatory Assessment in Ambulatory Boys with Nonsense Mutation Muscular Dystrophy Treated with Ataluren | |
Craig M McDonald, LJ Wei, Gary L Elfring, Panayiota Trifillis, Francesco Bibbiani, Marcio Souza, Joseph McIntosh, Stuart W Peltz, Francesco Muntoni |
Clinical profile and benefit from riboflavin in BVVL due to RFVT2 deficiency | |
Manoj Peter Menezes, Kayla Cornett, Gabrielle Donlevy, Joshua Burns |
Multiplex ligation-dependent probe amplification based SMN1 deletion analysis in 150-Indian patients with spinal muscular atrophy | |
Hansashree Padmanabha, Veeramani Preethish-Kumar, KIRAN POLAVARAPU, Saraswati Nashi, Seena Vengalil, Deepha Sekar, Nalini Atchyaram, Priya Thomas, KRISHNA GK |
Spinal Muscular Atrophy, a single centre experience | |
Ann Agnes Mathew |
EARLY CLINIC-ELCTROPHYSIOLOGICAL PREDICTORS OF POOR FUNCTIONAL OUTCOMEIN GBS | |
EKTA AGARWAL |
Duchenne Muscular Dystrophy a South Indian Perspective | |
Ann Agnes Mathew |
Explore evaluation methods of treatment efficacy on spinal muscular atrophy | |
kotaro yuge, Masao Suda, Ryuta Ishii, Takashi Ohya, Shinichiro Nagamitsu, Motomu Yoshida, Yushiro Yamashita |
Double-blinded Randomized Placebo Controlled trial of Valproate and levocarnitine in Children with Spinal Muscular Atrophy (aged 2-15years) | |
Sheffali Gulati, Biswaroop Chakrabarty, Jaya Shankar Kaushik, Ranjith Kumar Manokaran, Priyanka Madaan, Prabhjot Kaur, Madhulika Kabra, Sumita Bisoi, Sanjay Wadhwa, R M Pandey, Y K Gupta |
Prevalence of smooth muscle dysfunction among children with Duchenne muscular dystrophy | |
Ranjith Kumar Manokaran, Biswaroop Chakrabarty, Prashant Jauhari, Rakesh Kumar, Sandeep Aggarwala, Arun Gupta, Manisha Jana, R M Pandey, Sheffali Gulati |
Case series - congenital myasthenia gravis genotype and phenotype co-relation | |
Rujuta Joshi |
Hereditary Sensory and Autonomic Neuropathy Type VII- A Rare Presentation | |
Maroti Kadam, Swati Gupta, Mamta Muranjan, Rajwanti K Vaswani |
Etiological Profile of Hereditary Muscular Weakness in Pediatric Outpatients in Northern India | |
Prateek Kumar Panda, Prashant Jauhari, Biswaroop Chakrabarty, M C Sharma, Vaishali Suri, Chitra Sarkar, Madhulika Kabra, Sheffali Gulati |
Phenotype-Genotype correlation ofa cohort of children with genetically confirmed Congenital Myasthenic Syndrome | |
mukul malhotra, Karthik Muttusamy, Sangeetha Yoganathan, Maya Mary Thomas, Pavalan Paneer, sumita Danda |
Pulmonary functions in children with dystrophinopathy aged 5-18 years on oral steroid therapy for at least six months | |
Ankit Meena, Biswaroop Chakrabarty, Kana Ram Jat, S K Kabra, Sheffali Gulati |
Genetic evaluation of Congenital Myopathy (CM) and Congenital Muscular Dystrophy (CMD) in children : Slow Death of Muscle biopsies | |
RINI KOTHARI, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, PRASHANTHI ARIPRALA, RAMPRASAD VL, THENRAL SG |
Schwartz-Jampel syndrome responding positively to carbamazepine therapy: a case report and a novel mutation | |
Gürkan Gürbüz |
Anti –HMG-Co A reductase antibodies associated with progressive necrotizing myositis and autophagosomes in a teenager | |
Eleanor Ng, Maina Padmanabha Kava, Peter Williams Rowe, Simon Williams, Phillipa Lamont, Rei Curd Junckerstorff |
Clinical profile of three children with HSAN type 4 from South India | |
Beena Suresh, Beena Suresh, Sujatha Jagadeesh |
Guillain-Barré syndrome in a pediatric tertiary center (last five years) | |
Mafalda Sampaio, Cristina Garrido, Ruben Rocha, Marcio Cardoso, Ana Paula Sousa, Teresa Temudo, Sónia Figueiroa, Ines Carrilho, Manuela Santos |
McArdle disease: a diagnosis to suspect in the paediatric age | |
ruben Rocha, Cristina Garrido, Ana Cardoso, Manuela Santos |
Clinical and genetic characteristics of congenital myasthenia syndrome with episodic apnea caused by CHAT gene mutation in China | |
Zhimei Liu, Fang Fang |
Comparison of five different electrophysiological criteria for Childhood Guillian Barre Syndrome | |
ANANTHANARAYANAN KASINATHAN, Arushi Gahlot Saini, Renu Suthar, Lokesh Saini, Jitendra K Sahu, Pratibha Singhi, Sunit Singhi, Naveen Sankhyan |
A case series of hereditary sensory autonomic neuropathy in children | |
Renu Suthar, Hansa Shree Padmanabha, Arushi Gahlot Saini, Jitendra K Sahu, Bhavneet Bharti, Naveen Sankhyan, Ingo Kurth, Pratibha Singhi |
A Case of Congenital Myasthenia with False Positive Anti-acetylcholine Receptor antibody | |
Chee Geap Tay, Limin Li, Chin Seng Gan, Chee Ming Teh, Vigneswari Ganesan, Choong Yi Fong |
Clinical and genetic characteristics of GDAP1 gene mutation in Charcot Marie Tooth disease | |
JUN LAN LU, JUN LAN LU |
Somatosensory Evoked Potential: a normative study in children | |
DILIP THAKUR |
A pediatric case of anti-MuSK-antibody-positive ocular myasthenia gravis | |
Jeesuk Yu |
Paediatric Gullain Barre syndrome and its variants – observation of clinico-electrophysiological profile in a tertiary care hospital | |
Sufia Khatun Sumi |
Factors influencing initial diagnosis of Guillain Barre syndrome : A retrospective analysis | |
Padma Balaji, Vasanthi Thiruvengadam |
SHORT TERM NEUROLOGICAL OUTCOME OF A COHORT OF ACUTE ASYMMETRIC FLACCID MYELITIS | |
lokesh saini |
Disorders of Neuromuscular transmission in children: experience of a tertiary centre from North India | |
Priyanka Madaan, Biswaroop Chakrabarty, Prashant Jauhari, Aparajita Gupta, Rajni Farmania, Vishal Sondhi, Rachna Dubey, Sheffali Gulati |
Collagen VI related myopathies: clinical variability of triple-helical domain mutations of COL6A mutations | |
Sophelia HS Chan, Ka Yee Anna Kwong, Ho Ming Luk, Fai Man Ivan Lo, Tsui Hang Sharon Fung, Ho Yin Mandy Tsang, Ho Yin Brian Chung, On-Kei Angel Chan |
Clinicopathological profile and treatment outcome of Inflammatory myopathies in children: a retrospective cohort study | |
Prateek Kumar Panda, Vyshakh Anand, Prabhjoth Kaur, Prashant Jauhari, Biswaroop Chakrabarty, Atin Kumar, Manisha Jana, M C Sharma, Vaishali Suri, Chitra Sarkar, Sheffali Gulati |
Abnormalities of Fatty Acid Oxidation as Potential Candidate Biomarker for Spinal Muscular Atrophy (SMA) | |
Maina Padmanabha Kava |
Neonatal and Fetal Neurology
Head growth, brain growth and neurodevelopmental outcomes in preterm neonates | |
Thiviya Selvanathan, Vann Chau, Rollin Brant, Anne Synnes, Ruth Grunau, Steven Miller |
Myocardial dysfunction as predictor of neurodevelomental outcome in severely asphyxiated term neonates-A case control study. | |
Himani Bhasin, Arvind Saili, Sushma Nangia |
Health Related Quality of Life of Former Preterm Infants after Posthemorrhagic Hydrocephalus and Shunt Insertion | |
Haim Bassan, Moran Gigi, Jonathan Roth, Rina Eshel, Shlomi Constantini |
ROLE OF SUBCORTICAL INJURY IN NEONATAL STATUS EPILEPTICUS | |
Siddharth Jain |
Antenatal diagnosed Arachnoid Cyst [AAC]: An experience of 11 children | |
Naresh Biyani |
Antenatal diagnosed Spilt Cord Malformation type 1 [ASM]: An experience of 18 children | |
Naresh Biyani |
Association of amplitude integrated EEG findings with short term neurological outcome in term neonates | |
Giriraj Kumar Sharma, Padma Balaji, Vaanathi H, Shobna R, Rahul Yadav |
Application of Cerebral Function Monitor for electrical seizure-detection and neurological maturity assessment in Intrauterine Growth Restricted Neonates : A Pilot Study | |
Jyotindra Narayan Goswami, Ashutosh Kumar, Saroj Kumar Patnaik |
Fetal intraventricular haemorrhage (IVH), ventriculomegaly, cataracts and retinal haemorrhages due to Collagen 4A1 mutation | |
Prakash Satodia, Jerald William, Priya Parthasarathy |
Can nuchal cord be responsible for later neurodevelopmental disorders | |
Edina Karabeg, Enes Karabeg, Adi Karabeg, Biserka Rešić |
Why do neonates receive antiepileptics? | |
Abhijeet Anant Rakshasbhuvankar, Shripada Rao, Soumya Ghosh, Lakshmi Nagarajan |
The effect of Fetally Open, Fetoscopic and Postnatal Myelomeningocele Closure on Neuromuscular Outcome in Spina Bifida Aperta | |
Renate J Verbeek, Agnieszka Pastuszka, Tomasz Koszutski, Johannes H van der Hoeven, Eelco W Hoving, Deborah A Sival |
VICI SYNDROME- A RARE CASE REPORT | |
Giriraj Kumar Sharma, vaanathi H, padma balaji, shobana R, rahul anand yadav |
Normative data of ABR in newborns and young infants | |
monika chhajed, lokesh saini, Vrajesh Udani, Saranjit kaur |
A Prospective Observational Study of Neurodevelopmental Outcomes at One Year in Neonates receiving Family Centered Care in NICU | |
Arti Maria |
Long term prophylactic anticonvulsant uses on neurodevelopmental and neurophysiological outcome in asphyxiated neonate with encephalopathy | |
dipa saha |
Neurodevelopmental follow up in high risk babies – The scenario in India | |
Anasuya Das |
NEUROIMAGING FINDING OF CONGENITAL CHICKUNGUNYA ENCEPHALITIS | |
Deepak Dhami |
OUTCOME OF ISOLATED FETAL VENTRICULOMEGALY | |
Prakash Satodia, Soma Mukherjee |
Late MR Spectroscopy is not Recommended in the Evaluation of Neonatal Hypoxic Ischemic Encephalopathy (HIE). | |
Suhasini Kauskal, Christabel Lee, Paola Pergami |
SOCS3 a new link between Astrocyte and Fetal Alcohol Spectrum Disorder | |
Chen Yang |
Description of primary neurologic phenotypes in congenital CMV infection | |
Hitha Vishwanath Amin, Lisa Emrick, Gail Demmler-Harrison |
Neurodevelopmental Outcomes of Therapeutic Hypothermia from a NICU in Bangladesh | |
MA Mannan, AB Shilpi, Naila Z Khan |
Characteristics of exosomes in the cerebrospinal fluid of preterm infants | |
Robert Spaull, Bryony McPherson, Andriana Gialeli, Aled Clayton, James Uney, Oscar Cordero-Llana, Axel Heep |
Neurogenetics
Clinical and hereditary characteristics of MECP2 duplication syndrome in Chinese patients | |
zhanwen he, Xiangyang Luo, Liyang Liang |
Cerebral infarction, growth retardation and severe intellectual disability in Korean patients with de novo duplication of 14q32.2 | |
Ji Yoon Han, In Goo Lee |
Two Siblings with Congenital Myotonia carrying a New Mutation in the CLCN 1 Gene | |
Nezir Özgün |
Optic Atrophy and Retinal Pigmentary Changes: Expanding The Phenotypic Spectrum of Farber Lipogranulomatosis | |
Abdullah Saeed Alamri, Ali A AlFaiz, Daniah Alshowaeir, Fatimah Al Mousawi, Adel A Mahmoud, Aqeela Al-Hashim |
Expanded clinical spectrum of Okur-Chung neurodevelopmental syndrome in a patient with a hot sport mutation (p.Lys198Arg) in the CSNK2A1 gene. | |
Kohei Haraguchi |
The Landscape of Genetic causes of basal ganglia and thalamus involvement in children based on the first 5000 MRI studies | |
SAAD ALSHAHWAN |
Delineation of the CLP1 mutations; A possible founder mutation in Turkish cohort | |
Sema Saltik, Serhat Guler, Tanyel Zubarioglu, Ertugrul Kiykim, Cengiz Yalcinkaya, Gözde Yesil |
ISCA2 Related Mitochondrial Disorder: A distinct cause of Infantile Leucodystrophy | |
Sadia Tabassum, Rowim Al Mutairi, Mohammed Al Mannai, Ali Al Otaibi |
Two distinct phenotypes caused by the same mutation in the SAMHD1 gene | |
Serdal Gungor, Derya Okur, Elmasnur Yilmaz, Ana Topf, Rita Horvath, Hanns Lochmuller, Bilge Ozgor, Ece Sonmezler, Uluc Yis, Ahmet Yaramis, Yavuz Oktay, Semra Hiz |
NGS Analysis of four Chinese siblings with Late-Infantile Neuronal ceroid Lipofuscinosis | |
ren xiaotun |
Hereditary sensory and autonomic neuropathy(HSAN ) type IV in Jordan | |
amira masri |
CONSEQUITUR: A multinational effort towards determining the neurogenetic disease burden of consanguineous marriages in Turkey by genomics approaches | |
Semra Ayse Hiz, Elmasnur Yilmaz, Derya Okur, Ece Sonmezler, İpek Kalafatcilar, Serdal Gungor, Ahmet Yaramis, Uluc Yis, Erhan Bayram, Ana Topf, Rita Horvath, Hanns Lochmuller, Yavuz Oktay |
Pallister-Hall syndrome – case report | |
Himani Bhasin, Suvasini Sharma, Bijoy Patra |
The clinical features,laboratories characteristics and genetic diagnosis of Kabuki syndrome | |
Hong Mei Wang, Xiao-hui Wang, Hu-sheng Wu, Yun Wu, Xiu-wei Zhuo |
De novo KCNH1 mutation in an infant with Temple-Baraitser syndrome | |
Jun Hu |
Next Generation Sequencing Based Multi-gene Testing of Over 1000 Indian Patients Affected with Neurological Disorders Revealed an Improved (>40%) Diagnostic Yield | |
Ashraf U Mannan, Aparna Ganapathy, Avshesh Mishra, Anil Vittal Kanthi, Megha Rani Soni, Irene Patric, Aparajit Sridharan, Sobha George, Lakshmi Mohan, Swathi M Chinnappa, Ankitha Prabhudev, Syama Sreedharan, Thyagarajan Chandrasekaran, Priyanka K, Mukunth Sadagopan, Aswathy S L, Vidya H K, Satish Sankaran, Shanmukh Katragadda, Vamsi Veeramachaneni, Ramesh Hariharan, Vijay Chandru |
Rett (-like) syndrome: expanding the genetic sprectrum to KIF1A and GRIN1 gene | |
Jiaping Wang, Jiaping Wang, Qingping Zhang, Yan Chen, Shujie Yu, Xiru Wu, Xinhua Bao |
Clinical, Genetic and Follow-up Study of Leigh Syndrome in Children | |
Shen Danmin |
NDUFS6 mutations cause lethal neonatal mitochondrial complex I deficiency | |
MOHAMED ALJABRI |
The Clinical Profile of Tuberous Sclerosis Complex: A Retrospective Cohort Study in A Tertiary Care Hospital In Bangladesh | |
Md Mizanur Rahman, Kanij Fatema |
Clinical and Imaging Characteristics of Subependymal Giant Cell Astrocytoma in Patients with Tuberous Sclerosis Complex included in TOSCA – TuberOus SClerosis Registry to IncreAse Disease Awareness | |
Anna C Jansen, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D´Amato, Guillaume B d'Augères, Petrus J De Vries, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Rima Nabbout, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C Kingswood |
Burden of Illness and Quality of Life among Patients with Tuberous Sclerosis Complex: Findings from TOSCA Research Project | |
Anna C Jansen, Elena Belousova, Mirjana P Benedik, Tom Carter, Vincent Cottin, Paolo Curatolo, Maria Dahlin, Lisa D' Amato, Guillaume B d'Augères, Petrus J de Vries, José C Ferreira, Martha Feucht, Carla Fladrowski, Christoph Hertzberg, Sergiusz Jozwiak, John A Lawson, Alfons Macaya, Ruben Marques, Rima Nabbout, Finbar O’Callaghan, Jiong Qin, Valentin Sander, Matthias Sauter, Seema Shah, Yukitoshi Takahashi, Renaud Touraine, Sotiris Youroukos, Bernard Zonnenberg, John C Kingswood |
Mutation Screening using Next Generation Sequencing (NGS) Gene Panel in Patients with Normal Targeted Metabolic Profiling | |
MAJED J. Dasouki, Amal Jabr, Ghadah AlDakheel, Mohamed Abouelhoda, Shazia Subhani, Fahd Elbadoui, Nada AlTassan, Dorota Monies |
Genetic profile of childhood Charcot-Marie-Tooth disease | |
Stuart Murray, Joshua Burns, Leah Kim, Kayla Cornett, Manoj Menezes |
Phenotype and genotype features of twelve Chinese children with mitochondrial DNA depletion syndromes | |
Lifang Dai |
Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport | |
heba youssef el khashab, Farrukh ABBAS Chaudhry |
Aicardi-Goutières Syndrome - expanding the phenotypic spectrum. | |
Ami Shah, Snehal Mallakmir, Rashid Merchant, Mitusha Verma |
X linked infantile epileptic encephalopathy due to SMC1A truncating mutation - ‘An emerging phenotypic syndrome’ | |
Ami Shah, Neeta Naik, Salil Gundewar |
A Novel Missense Variant p.(Leu60Pro) in FAM126A Causes Leukodystrophy, Hypomyelinating, 5 | |
Aman Elwadhi, Suvasini Sharma, Bijoy Patra, Parneet Kaur, Katta M Girisha, Anju Shukla |
LAMA2 related congenital muscular dystrophies- Two case reports and correlation of genotype with clinical, molecular phenotype | |
SNEHAL MALLAKMIR, SNEHAL MALLAKMIR, Rashid Merchant, Vijay Yewale |
Phenotypic spectrum of Novel mutations in Paediatric mitochondrial disorders: A study from a tertiary care centre in Western Maharashtra. | |
Dr Sonam Rameshchandra Kothari, Dr Shilpa Kulkarni, Dr Leeha Singh, Dr Anaita Udwadia Hegde, Dr K N Shah |
Genotype and phenotype analysis of Leigh syndrome involving valine metabolism in 8 Chinese children | |
Xiaodi Han, Fang Fang, Zhimei Liu |
Genetic spectrum of Infantile epileptic encephalopathy: Indian experience | |
Spoorthi Jagadish, Rahul Badheka, Neelu Desai, Vrajesh Udani |
Collaborative data collection by TREAT-NMD Registries to support post-marketing surveillance in Spinal Muscular Atrophy | |
Michela Guglieri, Joanne Bullivant, Victoria Hodgkinson, Miriam Rodrigues, Volker Straub, Hugh Dawkins, Craig Campbell, Nathalie Goemans |
Clinical and Genetic Correlation in Childhood Onset Pharmacoresistant Epilepsy | |
Ami Shah, Neeta Naik, Abhinav Sahu, Abhinav Tiwari Tiwari |
Top 15 research priorities in tuberous sclerosis complex | |
Anna Jansen, Eva Schoeters, Alain Wouters, Peter Raeymaekers |
Next generation sequencing: a magic bullet or a cautious sword? | |
Shruti Bajaj, Mamta Muranjan, Anaita Hegde, Mukesh Agrawal |
Combining Pathway analysis and animal model behavioral testing for the identification of treatment for neurodevelopmental disorders | |
Francois Bolduc, Richard He, Kerri Whitlock, Cory Rosenfelt |
RHOBTB2 gene: recently discovered cause of rett-like encephalopathy, with possible therapeutic opportunity | |
Gia Melikishvili, Olivier Dulac, Nugzar Sekhniaidze, Mariam Melikishvili, Sophio Kakabadze, Nazi Tabatadze |
ATP1A3 mosaicism in families with alternating hemiplegia of childhood | |
Xiaoling Yang, Xiaoxu Yang, Shupin Li, Qi Zeng, Jing Zhang, August Yue Huang, Adam Yongxin Ye, Zhe Yu, Sheng Wang, Yuwu Jiang, Xiru Wu, Qixi Wu, Liping Wei, Yuehua Zhang |
Study of the rare causative genes and analysis of genotype-phenotype correlations of Dravet syndrome | |
Xiaojuan Tian, Qi Zeng, Jing Zhang, Aijie Liu, Xiaoling Yang, Yuwu Jiang, Xiru Wu, Yuehua Zhang |
The Study of Genotype-phenotype Correlation in Patients with Alternating Hemiplegia of Childhood | |
Shupin Li,, Xiaoling Yang, Jiaoyang Chen, Qi Zeng, Jing Zhang, Yuehua Zhang |
Therapeutic Antisense Oligonucleotides based Exon Skipping Gene Editing Strategies in Duchenne Muscular Dystrophy | |
Arun Shastry |
The mosaicism and incomplete penetrance of PCDH19 mutations | |
Aijie Liu, Xiaoxu Yang, Xiaoling Yang, Qixi Wu, Jing Zhang, Dan Sun, Zhixian Yang, Yuwu Jiang, Xiru Wu, Liping Wei, Yuehua Zhang |
HECW2 mutation causes periodic attacks of paralysis, intellectual disability and hypotonia | |
Kazuyuki Nakamura, Takahiro Abiko, Takashi Kanbayashi, Mitsuko Nakashima, Hirotomo Saitsu, Naomichi Matsumoto, Mitsuhiro Kato |
Holoprosencephaly and Kabuki’s syndrome | |
Surabhi Kaul, Rajan p Patel |
A good carpenter loves his tools: a case series highlighting the utility of the newer genetic tests | |
Shruti Bajaj, Shantala Vadeyar, Mamta Muranjan, Pradnya Gadgil, Kshitij Sheth |
A RARE TYPE OF HEREDITARY SENSORY AUTONOMIC NEUROPATHY | |
PRIYANKA SUNIL WALZADE, SHRUTI AGRAWAL, MANSI SHAH, VIRAJ SANGHI, SANGEETA RAVAT |
Developmental delay and cerebellar atrophy due to novel pathogenic variants in Gemin5 gene | |
Deepa Soundara Rajan |
NEUROLOGICAL AND EEG FINDINGS IN ANGELMAN SYNDROME:TALE OF 26 CHILDREN | |
Jeevan Silwal |
Gestalt Diagnosis of Children with Intellectual disability with Dysmorphism- Necessity for Establishing Genetic Diagnostic Approach. | |
Shaoli Sarker, Mustafa Mahbub, Narayan Saha, AZM AZAM, Humaira Rafiqa Quaderi, Shayla Imam Kanta, Sultana Razia, Fayaza Ahmed, Asma Hoque, Ahmed Asif Ferdous, Naila Zaman Khan |
Challenges in diagnosis and management of Acute Necrotising Encephalitis in a large South African family with RANBP2 mutation | |
Gillian Tracy Riordan, Alvin Ndondo, Sara Seneca, Karen Fieggen, Jo Wilmshurst |
CLINICAL PHENOTYPE IN PATIENTS WITH MEF2C MUTATION | |
Angeles Schteinschnaider, Julia Boccoli, Eliana Julian, Manuel Rivera, Paulina Carullo, Mercedes Villanueva |
Cockayne syndrome: Clinical and genetic study of a Maghrebian series | |
Thouraya Ben Younes, Ichraf kraoua, Hanene Benrhouma, Aida Rouissi, Hedia Klaa, Houda Yaakoub-Youssef, Najoua Miladi, Ilhem Ben Youssef-Turki |
Clinical profile, genetic correlation and treatment response in a cohort of children with genetically confirmed Early Infantile Epileptic Encephalopathy (EIEE) | |
Karthik Muthusamy, Sumita Danda, Sangeetha Yoganathan, Maya Thomas |
TELO2 Mutation in a Pair of Siblings -- a Rare cause of Global Development Delay / Epilepsy. | |
khian aun tan |
Subtle Seizure in the form of Recurrent apnoea Beyond Neonatal Period as Initial presentation of DIGEORGE Syndrome –A Rare Case Report . | |
BASUDEV BISWAL, TUSHITA GHOSH, rachita sarangi, ANUSPANDANA MAHAPATRA |
A founder homozygous mutation in VPS53 as the cause of Complicated Hereditary Spastic Paraparesis | |
Moran Hausman-Kedem, Shay Ben-Shachar, Shay Menascu, Liora Sagie, Aviva Fattal-Valevski |
Diagnostic yield of clinical exome sequencing in non-structural infantile onset epileptic encephalopathy | |
Prashant Jauhari, Prabhjot Kaur, Aparajita Gupta, Biswaroop Chakrabarty, Sheffali Gulati |
Assessment of cardiac involvement in childhood Neurofibromatosis Type 1 diagnoses, identification of Rasopathic cases | |
Ilyas Emre Tekdemir, Deniz Yüksel, Vehbi Dogan, Ayşe Aksoy, Hulya Kayılıoglu, Ulkuhan Oztoprak, Erhan Aksoy, Cigdem Sel |
Hereditary spastic paraplefgia (HSP) in Brazilian children: a clinical and genetic study. | |
Roberta Magalhães Ortega, Marcondes Cavalcante França Jr., Sergio Rosemberg |
A novel AP1S2 gene splice site mutation of X-linked mental retardation in a Chinese pedigree and literature review | |
Liang Huo |
Clinical and Genetic Spectrum of Disorders with Cerebellar Atrophy | |
Ramya Bandi, lokesh lingappa, Prasanthi Aripirala, Rini Kothari, Ramesh Konanki, Nikit Milind Shah, Smilu Mohanlal, Thenral SG, Ramprasad VL |
Copy Number Variant Sequencing reveals a 10q24.31-q24.32 haploid duplication in a Chinese family with congenital Split hand/foot malformation | |
LI GAO |
Mutation Analysis of genotype and clinical phenotype in children with hyperinsulinemic hypoglycemia | |
LI GAO |
Neuropsychological and behavioral characteristics of children with a candidate mutation in EMC10 - The characteristics of a new syndrome? | |
Eliana Haddad Eid, Tammy Pilowsky Peleg, Rachel Straussberg |
Modeling vanishing white matter disease with patient-derived induced pluripotent stem cell reveals astrocytic dysfunction | |
Ling Zhou, Peng Li, Na Chen, Lifang Dai, Yinan Liu, Li Shen, Jingmin Wang, Yuwu Jiang, Ye Wu |
Dysmorphology leading to the diagnosis of Schwartz Jampel Syndrome | |
Jayarekha Raja |
AicardiGoutieres - A close mimick of congenital infection: Case series with 3 children and 4 families | |
Beena Suresh, Sujatha Jagadeesh, Vaishnavi Reddy, Min Lee-Kirsch |
Novel homozygous mutations in NARS2 gene with mitochondrial dysfunction presenting as early infantile epileptic encephalopathy | |
Wilson Heredia |
Natural history and genotypic spectrum of cavitating leukoencephalopathy in childhood | |
Jie zhang, Ming Liu, Zhongbin Zhang, Ling Zhou, Weijing Kong, Yuwu Jiang, Jingmin Wang, Jiangxi Xiao, Ye Wu |
A study on protective effect of BDNF-MSC in Rett syndrome model | |
Hyo Jeong Kim, Jaesuk Lee, Delger Bayarasaikhan, Bonghee Lee |
Clinico-investigative profile of Hereditary spastic paraplegia in children | |
Mayank Vrujlal Detroja, Mahesh Kamate |
“STUDY OF CLINICO-ETIOLOGICAL PROFILE OF EARLY ONSET EPILEPTIC ENCEPHALOPATHY IN CHILDREN’’ | |
Boda Praful Kumar, LOKESH LINGAPPA, RAMESH KONANKI, NIKIT SHAH, RADHA RAMA DEVI, PRASHANTHI ARIPIRALA, THENRAL SG |
Whole Exome Sequencing in Diagnose of Patients with Leukodystrophy | |
Hsin Pei Wang, Wang-Tso Lee |
TITLE: Status of Genetic Counselling in Hereditary Neurogenetic disorders: A clinic-epidemiologic study in Western Rajasthan | |
Ankit Manoj Panday |
The spectrum of clinical findings, radiological profile and genetics of Vanishing White Matter Disease from tertiary care center of Southern India. | |
Syed Shah Naseeruddin Sarmast |
Developmental delay and cerebellar atrophy due to novel pathogenic variants in Gemin5 gene | |
Deepa Soundara Rajan |
TITLE: Spectrum of Neurocutaneous Disorders in Pediatric Neurology Clinic in Western Rajasthan | |
Ankit Manoj Panday |
Whole Exome Sequencing (WES) identifies PGAP3 mutation in three patients from two Saudi families with hyperphosphatasia with mental retardation syndrome 4 (HPMRS4) | |
ELSAYED MOHAMED ALI, HAMOUD MOHAMED GALLAB |
Infantile Neuroaxonal Dystrophy (INAD) in a Pair of Malaysian Siblings with Progressive Cerebellar Atrophy | |
Limin Li, Meow Keong Thong, Chee Geap Tay, Choong Yi Fong |
Rare chromosomal causes of developmental delay and epilepsy- Experience from a tertiary care center | |
Chaitanya Ashok Datar |
Preempting complications in genetic disorders: Lowe Syndrome a case study | |
Priyanka Dilip Patil |
Clinical and genetic studies on fifteen patients with tyrosine hydroxylase deficiency | |
Yao Zhang |
Juberg-Hellman Syndrome :X linked female restricted epilepsy in an extended family in North Kerala | |
Anilkumar Elayadeth, Divya Pachat, Akbar Mohamed |
Diversity of phenotypes in Infantile Seizure and their families with PRRT2 Mutations | |
TUNG MING CHANG, Inn Chi Lee, Ming Chen, Yuh Jyh Jong |
Phenotype plays an important role in the genetic diagnostic success rate in a cohort of 500 families with rare | |
Keri Ramsey |
XIA-GIBBS SYNDROME WITH PARTICULAR HAIR - A RARE CAUSE OF GLOBAL DEVELOPMENTAL DELAY | |
Diana Gabriela Barca, Cristina Minca, Mihaela Axente |
CHALLENGES IN CLINICAL INTERPRETATION OF NEW MUTATIONS IN RARE CONDITIONS | |
Diana Gabriela Barca, Sorina Mihaela Papuc, Carmen Burloiu, Aurora Arghir, Magdalena Budisteanu |
Molecular diagnosis and genetic counselling of X fragile Syndrome | |
Nouha Abdelmoula Bouayed, Sonda Kammoun, Fatma Abid, Balkiss Abdelmoula, Wafa Aloulou, Samir Aloulou |
Neurocritical care, Neurotrauma, Neuroprotection
Neurological Complications in Pediatric Cardiac Surgery: Incidence, Predictors and Outcome | |
wejdan salem hakami |
Our experience in the management of diffuse axonal injury patients in pediatric population and the review of literature- an institutional study. | |
Achal Gupta, Konika Bansal, Nitin Dange |
Assessment of clinical follow-up and prognosis in acute neurological condition in pediatric patients managed in pediatric intensive care unit | |
Ece Naz Karakaya, Deniz Yüksel, Selman Kesici, Ayşe Aksoy, Ülkühan Öztoprak, Çigdem Genç Sel, Erhan Aksoy, Hülya Kayılıoğlu |
Emergency room visits and admission rates of children with neuromuscular disorders: A 10-year experience in a medical center in Taiwan | |
Tai-Heng Chen, Yao-Hua Liu, Wei-Tsun Kao, Yung-Hao Tseng |
Diagnostic Utility of Middle Cerebral Artery flow indices as a Non-invasive tool for detecting Raised Intracranial Pressure in Pediatric patients. | |
Indar Kumar Sharawat, Naveen Sankhyan, Ananthanarayanan Kasinathan, Arun Bansal, Jitendra Kumar Sahu, Kushaljit Singh Sodhi, Mangat Ram Dogra |
Clinico-radiological profile of acute leucoencephalopathy with restricted diffusion- a novel cause of acute encephalopathy in children. | |
Mahesh Kamate |
Early Post-Traumatic Seizures in PediatricTraumatic Brain Injury | |
Snehal Surana, Arpita Devbrata Adhikari, Vineet Kumar, Mona Gajre, Vidya M |
Big Black Brain | |
Sayoni Roy Chowdhury, Rajwanti K Vaswani, Chandrahas Deshmukh, Jane David, Anupa Johny Ekka |
Native medicine use and lead poisoning in children | |
Renee Alce, Renee Alce, Padma Balaji, Ravikumar Krupanandan, Venkataraman Viswanathan, Bala Ramachandran |
Neuroprotective effects of vitamine D in hiperoxic brain injury | |
erhan bayram, ipek polat, serap cilaker mıcılı, Meryem Calısır, Uluç Yiş, Guven Erbil, Osman Yılmaz, semra hız kurul |
A prospective study on incidence of non-convulsive status epilepticus in children with acute encephalopathy | |
sruthi thiruveedi, Dr Lokesh Lingappa, Dr Ramesh Konanki, Dr Nikit shah, Dr Anupama yerra, Dr Farhan Shaikh |
Brain Death Determination for Comatose Patients in The Pediatric Intensive Care Unit | |
Kun-Long Hung, Su-Ching Hu, Wong Lee-Chin |
Neuroradiology
Cranial Magnetic Resonance Imaging patterns in infants with hypernatremic dehydration | |
Gouri Rao Passi, Shailesh Gupta, Puneet Yadav |
Congenital Brain and Spine Malformations – prenatal fetal MRI approach | |
Ivana Markovic |
Value of Neuroimaging in Thalassemia | |
Amitkumar Jayant Choudhari, Rashid Merchant, Deepak Patkar, Mitusha Verma, Alka Karnik |
pseudo TORCH syndrome – Recessive mutation in occludin ( OCLN ) gene | |
shriganesh patil |
Intracerebral large artery disease with Aicardi-Goutières Syndrome | |
Chung Jane Ng, Wang Tso Lee |
Role of Fetal Neuroimaging in Congenital Cytomegalovirus Infection, with Postnatal Imaging Correlation. | |
Vinay Kandula, Rahul Nikam, Lauren Averill, Arabinda Choudhary |
Clinical & Neuro-Imaging Changes of Subacute sclerosing panencephalitis- Experience 30 Cases in Tertiary Care Center in Bangladesh | |
Gopen Kumar Kundu |
Case Report: Van der Knaap Disease | |
Vaishali Deshpande, Vaishali Deshpande, Sushma Save, Sandeep Bavdekar |
NCL11:A rare cause of pure pancerebellar atrophy | |
Mahesh Kamate |
Distribution of Cerebellar Tonsillar Position in the Indian Pediatric Population | |
Divyata R Hingwala |
Neuroimaging findings in Neuromyelitis Optica spectrum disorder and mimics | |
Divyata R Hingwala |
Brain MRI in children with Wilson Disease | |
yuan wu, Ying Zhu, Ting Zhang, Ming Li |
Isolated mitochondrial complex IV (cytochrome c oxidase) deficiency mimicking ADEM | |
Amal Yousef Kentab, Mohammed Al-Nasser, Hamdy Hassan, Hisham El Khaldi |
Neuroimaging in paediatric central nervous system infections. | |
Dr.Deepak Patkar, Dr. Amitkumar Choudhari, Amit kumar Pandey, Dr. Shilpa Kulkarni, Dr. Rashid Merchant |
Pituitary iron and volumetric analysis in β Thalassemia | |
Dr. Anuja Nayak, Dr. Deepak Patkar, Dr. Amitkumar Choudhari, Dr. Shilpa Kulkarni, Dr. Rashid Merchant |
cerebellar calcification and seizures in a child with autoimmune polyendocrine syndrome 3A | |
Rachel Peterson, Asha Kuruvilla, Ann Mathew |
Clinical & Neuro-Imaging Changes of Subacute sclerosing panencephalitis- Experience 30 Cases in Tertiary Care Center in Bangladesh | |
Gopen Kumar Kundu |
Vacuolar leukodystrophy revealing COX10 mutation | |
Thouraya Ben Younes, Hanene Benrhouma, Rania Ben Aoun, Lilia Kraoua, Said Galai, Hedia Klaa, Aida Rouissi, Ridha Mrad, Cyrine Drissi, Souhail Omar, Abdelhamid Slama, Ichraf Kraoua, Ilhem Ben Youssef-Turki |
Spectrum of acquired White Matter Disorders in Children and their Outcomes | |
Vikas Chauhan, Arushi Gahlot Saini, Naveen Sankhyan, Sameer Vyas, Paramjit Singh, Jayashree Muralidharan |
Pineal cysts in children: the experience of child neurology department | |
sirine belghuith |
RHOMBENCEPHALO SYNAPSIS – A RARE CEREBELLAR ANOMALY WITH GOMEZ LOPEZ HERNANDEZ SYNDROME | |
Leema Pauline Cornelius |
ne imaging of children with Tuberous sclerosis complex: is it safe to adapt international recommendations for resource limited settings? | |
Marie Wessels, Bergit Schlegel, Jo M Wilmshurst |
ALERD In a Post-Operative Case Of a 20 Month Girl Child. | |
Narendranadha reddy k, MAHESH KAMATE, MAYANK DETROJA, santosh kurbeit |
The spectrum of leukodystrophies in children: Experience at a tertiary care centre from North India | |
Biswaroop Chakrabarty, Priyanka Madaan, Puneet Jain, Sachendra Badal, Prashant Jauhari, Atin Kumar, Manisha Jana, Neerja Gupta, Madhulika Kabra, Sheffali Gulati |
Clinical correlates of mineralizing lenticulostriate vasculopathy (mLSV) in children | |
Jatinder Singh Goraya |
POMS 2b pediatric cohort): Effect of Auto-adjusting Continuous Positive Airways Pressure on cognition and MRI in children with Sickle Cell Disease: a single-blind, randomized, controlled phase II trial | |
Satwinder Sahota, Jamie Kawadler, Hanne Stotesbury, Melanie Koelbel, April Slee, Dawn Saunders, Fenella Kirkham |
Neuroimmunology
Autoantibodies normilize after a month in tonsilitis and persist in Sydenham's chorea | |
Hilla Ben-Pazi, Julie Stoner, Adi Aran, Kathy Alvarez, Madeleine W Cunningham |
Efficacy of thyrotropin releasing hormone therapy for patients with subacute sclerosing panencephalitis | |
Eiji Nakagawa |
A NEW NEUROINFLAMMATORY DISORDER IN CHILDREN: Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids (CLIPPERS) | |
tarishi nemani, PURVA KENI KARNAVAT, EPARI SRIDHAR, ANAITA UDWADIA HEGDE |
MicroRNA-181a-5p regulates blood brain barrier permeability after meningoencephalitis via positive regulating HMGB1 expression | |
Ling-juan Liu |
Unsolved mystery:11-year-old patient with antibody negative immune-mediated necrotizing myopathy | |
Cemal Karakas, Jeetendra Sah, Yaacov Anziska, Yoshimi Hisamoto, Radha Giridharan, Joan Cracco, Alexandra Reznikov, Geetha Chari |
Paediatric Guillian-Barré Syndrome variants presenting with dysautonomia | |
Omar Abdel-mannan, Luigi D’Argenzio, Matthew Pitt, Felice D’Arco, Sanjay Bhate, Yael Hacohen, Marios Kaliakatsos |
Hemophagocytic Lymphohistiocytosis: A missed diagnosis in children with neurological manifestations | |
Marwa Saeed Abd Elmaksoud, Ahmed Adel Hassan Elbehairy, Asmaa Elsharkawy, Yasmine El Chazli |
Anti-MOG antibody related demyelinating diseases: Clinical-radiological spectrum and treatment experience | |
Hepsen Mine SERIN, Erdem Simsek, Seda Kanmaz, İpek Dokurel Cetin, Sanem Yılmaz, Gul Aktan, Hasan Tekgul, Sarenur Gokben |
Clinical and prognostic analysis of ocular myasthenia gravis in children | |
Chen Jiji, Jiang Li, Li Xiujuan, Hong Siqi |
clinical features of Myelin oligodendrocyte glycoprotein(MOG)antibody positive cetral nervous system inflammatory dymyelination in 31 children | |
Zhang wh |
Therapeutic plasma exchange in inflammatory demyelinating CNS syndromes in paediatric patients | |
Silvia Noemi Tenembaum, Andrea Savransky, Marina Huaman Rios, Silvana Liz Vergel, Mabel Castro Velasquez, Sara Perez Sierra, Gabriela Marcarian, Romina Alba, Ana Maria Pugliese |
Effect of fingolimod in pediatric MS: further insights from sensitivity, supportive and post-hoc analyses from PARADIGMS | |
Kumaran Deiva, Peter Huppke, Brenda Banwell, Tanuja Chitnis, Jutta Gärtner, Lauren Krupp, Emmanuelle Waubant, Tracy Stites, Gregory Lewis Pearce, Martin Merschhemke |
OPSOCLONUS-MYOCLONUS SYNDROME: SIMULTANEOUS COMBINATION IMMUNOSUPPRESSIVE THERAPY WITH EXCELLENT OUTCOME | |
Shailesh Barot, Anaita Hegde, Krupa Torne, Manohar Patil, Vaibhavi Barot |
FATAL DIAGNOSIS OF SSPE TO TREATABLE CAUSE OF AUTOIMMUNE ENCEPHALITIS | |
chandra sadanandavalli retnaswami |
Improved performance of the 2017 McDonald criteria for diagnosis of multiple sclerosis in children irrespective of age | |
yael hacohen, Wallace Brownlee, Kshitij Mankad, WK 'Kling' Chong, Ming Lim, Evangeline Wassmer, cheryl Hemingway, Fredrik Barkhof, Olga Ciccarelli |
Pediatric-onset multiple sclerosis in Egypt: a multi-center registry | |
AMR MOHAMMED |
Spinal cord disease following Falls and minor Sporting injury: Myelitis or SCIWORA? | |
Terrence Thomas |
case series of pediatric multiple sclerosis | |
Yareeda Sireesha, Angamattu Kanikannan, Mathukumalli Neeharika |
Inflammatory neuropathology of infantile Alexander disease: A case report | |
Kengo Kora, Takeo Kato, Minako Ide, Takayuki Tanaka, Tomokatsu Yoshida |
Iatrogenic Intracranial Hypertension secondary to Immunoglobulin therapy of Chronic Inflammatory Demyelinating Polyneuropathy | |
Elizabeth Pilley, Conrad Schmoll, Jayakara Shetty, Kenneth McWilliam |
Pediatric Acquired Demyelination Syndromes (ADS) profile in a Brazilian center | |
José Albino da Paz, Renata Paolilo, Samira Apostolos-Pereira, Dagoberto Callegaro, Ana Luiza Araújo, Douglas Sato, Carolina Medeiros Rimkus |
Acquired neuromyotonia in children with CASPR2 antibodies | |
SNEHAL SURANA |
Subacute meningitis / Prolonged fever as presentations of MOG antibody associated autoimmune demyelination syndrome – a case series | |
Rahul Badheka, Vrajesh Udani, Neelu Desai |
AUTOIMMUNE ENCEPHALITIS: OUTCOMES IN A PEDIATRIC POPULATION | |
MONICA elsa FERREA, Paola Di Lalla, Laura Silvina Fernandez, Silvia Intruvini |
Chronic Lymphocytic Inflammation With Pontine Perivascular Enhancement Responsive To Steroids (CLIPPERS) | |
Manish Prasad |
Pediatric autoimmune encephalitis: Case series from two Chinese tertiary pediatric neurology centers | |
Jianzhao Zhang, Yuwu Jiang, Jianzhao Zhang |
Rare cause of intractable vomiting: Neuromyelitis Optica | |
Reena Jain, nirupa chandorkar, dinesh raj, pankaj vohra, suvasini sharma |
Retrospective study of 30 patients with Opsoclonus-Myoclonus Syndrome (OMS) in Brazil. | |
José Albino da Paz, Renata Paolilo, Ciro Matsui |
Clinical profile and outcome of Acute Necrotizing Encephalopathy of Childhood (ANEC): a retrospective cohort study from a tertiary care centre of North India | |
Sachendra Badal, Prateek Kumar Panda, Priyanka Madaan, Ankita Pal, Prashant Jauhari, Biswaroop Chakrabarty, Vishal Sondhi, Rachana Dubey, Sheffali Gulati |
Clinical and Neuroradiological profile of Acute Disseminated Encephalomyelitis in 13 children at tertiary center in Saudi Arabia | |
Amal Yousef Kentab, Amal Y. Kentab, Mustafa AM. Salih, Hamdy H. Hassan, Mohammed Na N. Al-Nasser, Heba Y. El khashab |
Intravenous immunoglobulin versus methyl prednisolone in children with ADEM:: a randomized controlled trial | |
Rajniti Prasad, Gautam Goswami |
Pediatric anti-NMDA receptor encephalitis: experience of a tertiary care teaching center in North India | |
Biswaroop Chakrabarty, Prateek Kumar Panda, Prashant Jauhari, Vishal Sondhi, Rachana Dubey, Sheffali Gulati |
Clinico-epidemiological profile of Opsoclonus Myoclonus Ataxia syndrome: experience of a tertiary care centre from north India | |
Biswaroop Chakrabarty, Prabhjot Kaur, Prashant Jauhari, Vishal Sondhi, Rachana Dubey, Prateek Kumar Panda, Sheffali Gulati |
Spectrum of Guillian Barre syndrome in children – atypical features, types, prognostic indicators and relationship to zika virus. | |
Ishita Tewari, Chandrakanta Kumar, Ravindra Garg, Amita Jain, Rashmi Kumar |
The case of Kinsburn`s Encephalopathy in a child with neuroblastoma of posterior mediastinum | |
Tetiana Stetsenko |
Pathognomonic features and Neuropsychiatric Outcome of Anti-NMDAR Encepahlitis in children: A case series | |
Janaki Menon, Veena Nair, Purushothaman Kuzhukkathukandiyil |
Brain stem encephalitis in children | |
Kavita P Thakkar, Yoshimi Sogawa, Amy C Goldstein, Giulio Zuccoli |
Our experience with Rituximab in two patients with anti-MuSK positive Myasthenia gravis. | |
MESUT GUNGOR, BULENT KARA, AYFER SAKARYA GUNES |
Follow-up Study on Chinese children with relapsing MOG-IgG-associated Central Nervous System demyelination | |
Ji Zhou, Xiaopeng Lu, Yao Zhang, Taoyun Ji, Yiwen Jin, Min Xu, Yuehua Zhang, Xinhua Bao, Hui Xiong, Xinzhi Chang, Yuwu Jiang, Ye Wu |
Clinico-radiological correlation of Acquired Demyelination Syndromes(ADS) of central nervous system: A pediatric cohort | |
ANSHITA ARORA, SONAM KOTHARI, SHILPA KULKARNI, ANAITA HEGDE, KRISHANKUMAR SHAH |
Intracranial Calcification, Spastic Paraparesis, Length Shortening and Immunological Disorders: Three SPENCDI Cases | |
MESUT GUNGOR, AYFER SAKARYA GUNES, BULENT KARA |
Acquired Central Nervous System demyelinating syndromes in children: experience of a tertiary centre from North India | |
Priyanka Madaan, Biswaroop Chakrabarty, Prateek Kumar Panda, Juhi Gupta, Vishal Sondhi, Rachana Dubey, Atin Kumar, Manisha Jana, Sheffali Gulati |
Acquired neuromyotonia in children with CASPR2 antibodies | |
Snehal Surana, Ratna Kumar, Prab Prabhakar, Matthew Piit, Yael Hacohen, Sukhvir Wright |
Clinico-radiologic spectrum and outcome of pediatric demyelinating disorders – A retrospective study | |
Bidisha Banerjee, Muhammed Valikandy Hafis, Ullas V Acharya |
Long term Outcome of Thymectomy in Pediatric Myasthenia Gravis | |
leeha Singh, Leeha Singh, Shilpa Kulkarni, Anaita Hegde, K. N. Shah |
Opsoclonus myoclonus ataxia syndrome: A study from a tertiary care center in Western India | |
leeha Singh, Shilpa Kulkarni, Anaita Hegde, K. N. Shah |
Low seropositivity to antiganglioside antibodies in Guillain-Barre Syndrome; A Prospective study of 83 children | |
Naveen Sankhyan, Sunit Singhi, Pratibha Singhi, Savita Verma, Mini Tageja |
Use of the radiotracer 18F-GE180 for PET scan imaging of active neuro-inflammation in children with multiple sclerosis | |
Badal G Jain, Hua Li, Zhang Shaohui, Xuyi Yue, Rahul Nikam, Alana Salvucci, Yangchun Xin, Diane Chugani, Harry Chugani |
Familial acute necrotizing encephalopathy (ANE1) | |
Zoltan Liptai, Sarolta Dobner, Peter Benke, Anna Szocs, Judit Moser, Fleur Vansenne |
Anti NMDAr antibody mediated encephalitis: unusual presentation with focal motor deficits: 2 case reports | |
pradnya gadgil, Nilima Bhalerao, Sunita Venkatraman |
Role of Rituximab and pulse Cyclophosphomide in anti-NMDAR encephalitis | |
Lakshminarayanan Kannan |
CLINICAL PROFILE, TREATMENT AND OUTCOME IN CHILDREN WITH NMDA RECEPTOR ENCEPHALITIS: DATA FROM A TERTIARY CARE MEDICAL COLLEGE IN KERALA. | |
abhishek ravindra jain, mini sreedharan, P A Mohammed Kunju, mary iype, bindu thankappan, ishita deasi, rajagembeeran venugopal, priyanka ramteke, heena sheikh |
Radiologically isolated syndrome in childhood: experience of our clinic | |
Ayfer Sakarya Güneş |
The Clinical Course of Children Younger than 7 Years of Age with Anti-N-methyl-D-aspartate Receptor Encephalitis | |
Hitha Vishwanath Amin, Sarah R Risen, Mered Parnes, Christian Michael Niedzwicki, Eyal Muscal |
Neurosurgery
Feasibility of using transcranial magnetic stimulation (TMS) for presurgical language mapping in young children | |
Shalini Narayana, Katherine K Schiller, Luke M Embury, Stephen Fulton, Amy McGregor, Basanagoud Mudigoudar, Sarah Weatherspoon, James W Wheless, Frederick Boop |
Dermoid cyst mimicking Gastro esophageal reflux disease | |
Surabhi Kaul, Stephen Katzen, Andrew Minzenmayer, Andrew Fang, Nivedita Thakur, Manish N Shah, Rajan P Patel |
Acalvaria: a 5-months follow up | |
Ivan Riyanto Widjaja, Angelina Armine Susanto Putri, Dicky Adi Putra, Marsha Zaneta, Nur Hasan |
Infected Dermal Sinus with Arachnoiditis (IDSA): An experience of 20 children | |
Naresh Biyani |
Functional mapping of the brain by novel tripolar EEG electrodes | |
Sameer C Dhamne, Damon Hyde, Shunan Li, Walt Besio, Alexander Rotenberg |
Utility of neuronavigated transcranial magnetic stimulation (nTMS) for functional motor mapping in infants and toddlers | |
Harper Lee Kaye, Gabrielle Block, Saeed Kayhanian, Hannah Purtell, Ugur Damar, Alexander Rotenberg |
Neurooncology
A randomized, double-blind, parallel group, placebo-controlled trial of metformin in tuberous sclerosis complex | |
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